Canonical Allele Identifier: CA375686381

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131688C>G (hg19) ; chr9:g.133256301C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256301C>G , CM000671.2:g.133256301C>G	GRCh38
NC_000009.11:g.136131688C>G , CM000671.1:g.136131688C>G	GRCh37
NC_000009.10:g.135121509C>G	NCBI36
NG_006669.1:g.21367G>C
NG_006669.2:g.23915G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.459G>C
ENST00000647353.1:n.54-5149G>C
ENST00000651471.1:n.385G>C
ENST00000679909.1:c.28+18861G>C	ENSP00000506089.1:n.28+18861G>C
ENST00000453660.3:n.441G>C
ENST00000538324.2:c.427G>C	ENSP00000483018.1:p.Gly143Arg
ENST00000611156.4:c.427G>C	ENSP00000483265.1:p.Gly143Arg
NM_020469.2:c.430G>C	NP_065202.2:p.Gly144Arg
NM_020469.3:c.430G>C	NP_065202.2:p.Gly144Arg