Canonical Allele Identifier: CA5305686

Gene: ABO

Linked Data

• dbSNP Id: rs56346931
• ExAC: 9:136131192 T / C
• gnomAD v2: 9-136131192-T-C
• gnomAD v3: 9-133255805-T-C
• gnomAD v4: 9-133255805-T-C
• MyVariant Identifiers: chr9:g.136131192T>C (hg19) ; chr9:g.133255805T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255805T>C , CM000671.2:g.133255805T>C	GRCh38
NC_000009.11:g.136131192T>C , CM000671.1:g.136131192T>C	GRCh37
NC_000009.10:g.135121013T>C	NCBI36
NG_006669.1:g.21863A>G
NG_006669.2:g.24411A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.955A>G
ENST00000647353.1:n.54-4653A>G
ENST00000679909.1:c.28+19357A>G	ENSP00000506089.1:n.28+19357A>G
ENST00000453660.3:n.937A>G
ENST00000538324.2:c.923A>G	ENSP00000483018.1:p.Tyr308Cys
ENST00000611156.4:c.923A>G	ENSP00000483265.1:p.Tyr308Cys
NM_020469.2:c.926A>G	NP_065202.2:p.Tyr309Cys
NM_020469.3:c.926A>G	NP_065202.2:p.Tyr309Cys