Canonical Allele Identifier: CA591309667

Gene: ABO

Linked Data

• dbSNP Id: rs990919088
• gnomAD v2: 9-136135482-T-G
• MyVariant Identifiers: chr9:g.136135482T>G (hg19) ; chr9:g.133260078T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260078T>G , CM000671.2:g.133260078T>G	GRCh38
NC_000009.11:g.136135482T>G , CM000671.1:g.136135482T>G	GRCh37
NC_000009.10:g.135125303T>G	NCBI36
NG_006669.1:g.17572A>C
NG_006669.2:g.20137A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-212A>C
ENST00000647353.1:n.54-8926A>C
ENST00000651471.1:n.191-212A>C
ENST00000679909.1:c.28+15084A>C	ENSP00000506089.1:n.28+15084A>C
ENST00000453660.3:n.168-212A>C
ENST00000538324.2:c.156-212A>C	ENSP00000483018.1:n.156-212A>C
ENST00000611156.4:c.156-212A>C	ENSP00000483265.1:n.156-212A>C
NM_020469.2:c.156-212A>C	NP_065202.2:n.156-212A>C
NM_020469.3:c.156-212A>C	NP_065202.2:n.156-212A>C