Canonical Allele Identifier: CA375686181

Gene: ABO

Linked Data

• gnomAD v4: 9-133256198-T-G
• MyVariant Identifiers: chr9:g.136131585T>G (hg19) ; chr9:g.133256198T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256198T>G , CM000671.2:g.133256198T>G	GRCh38
NC_000009.11:g.136131585T>G , CM000671.1:g.136131585T>G	GRCh37
NC_000009.10:g.135121406T>G	NCBI36
NG_006669.1:g.21470A>C
NG_006669.2:g.24018A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.562A>C
ENST00000647353.1:n.54-5046A>C
ENST00000651471.1:n.488A>C
ENST00000679909.1:c.28+18964A>C	ENSP00000506089.1:n.28+18964A>C
ENST00000453660.3:n.544A>C
ENST00000538324.2:c.530A>C	ENSP00000483018.1:p.Tyr177Ser
ENST00000611156.4:c.530A>C	ENSP00000483265.1:p.Tyr177Ser
NM_020469.2:c.533A>C	NP_065202.2:p.Tyr178Ser
NM_020469.3:c.533A>C	NP_065202.2:p.Tyr178Ser