Product Details

SNP ID

rs11152546

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:2788903 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAGCTCATGGTAAACTTGAGGAAC[A/G]TGCAAAAGTCATTGCAAAAAGTTTT

Phenotype

MIM: 300879

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

XG PubMed Links

Gene Details

Gene

XG

Gene Name

Xg blood group

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001141919.1		Intron			NP_001135391.1
NM_001141920.1		Intron			NP_001135392.1
NM_175569.2		Intron			NP_780778.1
XM_005274587.3		Intron			XP_005274644.1
XM_011545575.2		Intron			XP_011543877.1
XM_017029787.1		Intron			XP_016885276.1

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