Canonical Allele Identifier: CA375682186

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130995C>A (hg19) ; chr9:g.133255608C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255608C>A , CM000671.2:g.133255608C>A	GRCh38
NC_000009.11:g.136130995C>A , CM000671.1:g.136130995C>A	GRCh37
NC_000009.10:g.135120816C>A	NCBI36
NG_006669.1:g.22060G>T
NG_006669.2:g.24608G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1152G>T
ENST00000647353.1:n.54-4456G>T
ENST00000679909.1:c.28+19554G>T	ENSP00000506089.1:n.28+19554G>T
ENST00000453660.3:n.1134G>T
ENST00000538324.2:c.1116G>T	ENSP00000483018.1:p.Trp372Cys
ENST00000611156.4:c.*58G>T	ENSP00000483265.1:n.*58G>T
NM_020469.2:c.*58G>T	NP_065202.2:n.*58G>T
NM_020469.3:c.*58G>T	NP_065202.2:n.*58G>T