Product Details

SNP ID
rs1049938
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.7:26190552 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TCAGTGGTGGTCTTAGGATCAAAGA[A/C]GACTCATTGGTGTATAGAGTAAGCC
Phenotype
MIM: 600124 MIM: 604135
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
HNRNPA2B1 PubMed Links
Additional Information
For this assay, SNP(s) [rs17153378] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
HNRNPA2B1
Gene Name
heterogeneous nuclear ribonucleoprotein A2/B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002137.3 3086 UTR 3 NP_002128.1
NM_031243.2 3086 UTR 3 NP_112533.1
XM_005249729.1 3086 Intron XP_005249786.1
XM_017012109.1 3086 UTR 3 XP_016867598.1
XM_017012110.1 3086 Intron XP_016867599.1
Gene
NFE2L3
Gene Name
nuclear factor, erythroid 2 like 3
There are no transcripts associated with this gene.

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