Canonical Allele Identifier: CA5305736

Gene: ABO

Linked Data

• dbSNP Id: rs782380410
• ExAC: 9:136131324 T / C
• gnomAD v2: 9-136131324-T-C
• gnomAD v4: 9-133255937-T-C
• MyVariant Identifiers: chr9:g.136131324T>C (hg19) ; chr9:g.133255937T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255937T>C , CM000671.2:g.133255937T>C	GRCh38
NC_000009.11:g.136131324T>C , CM000671.1:g.136131324T>C	GRCh37
NC_000009.10:g.135121145T>C	NCBI36
NG_006669.1:g.21731A>G
NG_006669.2:g.24279A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.823A>G
ENST00000647353.1:n.54-4785A>G
ENST00000679909.1:c.28+19225A>G	ENSP00000506089.1:n.28+19225A>G
ENST00000453660.3:n.805A>G
ENST00000538324.2:c.791A>G	ENSP00000483018.1:p.Tyr264Cys
ENST00000611156.4:c.791A>G	ENSP00000483265.1:p.Tyr264Cys
NM_020469.2:c.794A>G	NP_065202.2:p.Tyr265Cys
NM_020469.3:c.794A>G	NP_065202.2:p.Tyr265Cys