Canonical Allele Identifier: CA467853088

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131296C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255909C>G , CM000671.2:g.133255909C>G	GRCh38
NC_000009.11:g.136131296C>G , CM000671.1:g.136131296C>G	GRCh37
NC_000009.10:g.135121117C>G	NCBI36
NG_006669.1:g.21759G>C
NG_006669.2:g.24307G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.851G>C
ENST00000647353.1:n.54-4757G>C
ENST00000679909.1:c.28+19253G>C	ENSP00000506089.1:n.28+19253G>C
ENST00000453660.3:n.833G>C
ENST00000538324.2:c.819G>C	ENSP00000483018.1:p.Val273=
ENST00000611156.4:c.819G>C	ENSP00000483265.1:p.Val273=
NM_020469.2:c.822G>C	NP_065202.2:p.Val274=
NM_020469.3:c.822G>C	NP_065202.2:p.Val274=