Canonical Allele Identifier: CA375686123

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131559G>C (hg19) ; chr9:g.133256172G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256172G>C , CM000671.2:g.133256172G>C	GRCh38
NC_000009.11:g.136131559G>C , CM000671.1:g.136131559G>C	GRCh37
NC_000009.10:g.135121380G>C	NCBI36
NG_006669.1:g.21496C>G
NG_006669.2:g.24044C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.588C>G
ENST00000647353.1:n.54-5020C>G
ENST00000651471.1:n.514C>G
ENST00000679909.1:c.28+18990C>G	ENSP00000506089.1:n.28+18990C>G
ENST00000453660.3:n.570C>G
ENST00000538324.2:c.556C>G	ENSP00000483018.1:p.Arg186Gly
ENST00000611156.4:c.556C>G	ENSP00000483265.1:p.Arg186Gly
NM_020469.2:c.559C>G	NP_065202.2:p.Arg187Gly
NM_020469.3:c.559C>G	NP_065202.2:p.Arg187Gly