Canonical Allele Identifier: CA467782914

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131641C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256254C>G , CM000671.2:g.133256254C>G	GRCh38
NC_000009.11:g.136131641C>G , CM000671.1:g.136131641C>G	GRCh37
NC_000009.10:g.135121462C>G	NCBI36
NG_006669.1:g.21414G>C
NG_006669.2:g.23962G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.506G>C
ENST00000647353.1:n.54-5102G>C
ENST00000651471.1:n.432G>C
ENST00000679909.1:c.28+18908G>C	ENSP00000506089.1:n.28+18908G>C
ENST00000453660.3:n.488G>C
ENST00000538324.2:c.474G>C	ENSP00000483018.1:p.Val158=
ENST00000611156.4:c.474G>C	ENSP00000483265.1:p.Val158=
NM_020469.2:c.477G>C	NP_065202.2:p.Val159=
NM_020469.3:c.477G>C	NP_065202.2:p.Val159=