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- SNP ID:
- rs74704112
- Gene
-
ABCG2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 88092868 - 88092868 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
GCTCTTACAGTACTCTTTACGCTTA[A/C]AAATAGCCATAAAAAACAACACAGG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603756
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Literature Links: |
ABCG2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| ABCG2 - ATP binding cassette subfamily G member 2 (Junior blood group) | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001257386.1 | Intron | NP_001244315.1 | ||||
| NM_004827.2 | Intron | NP_004818.2 | ||||
| XM_005263354.3 | Intron | XP_005263411.1 | ||||
| XM_005263355.3 | Intron | XP_005263412.1 | ||||
| XM_005263356.3 | Intron | XP_005263413.1 | ||||
| XM_011532420.2 | Intron | XP_011530722.1 | ||||
| XM_017008852.1 | Intron | XP_016864341.1 | ||||
| XM_017008853.1 | Intron | XP_016864342.1 | ||||
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