Canonical Allele Identifier: CA375686850

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136133502T>G (hg19) ; chr9:g.133258112T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258112T>G , CM000671.2:g.133258112T>G	GRCh38
NC_000009.11:g.136133502T>G , CM000671.1:g.136133502T>G	GRCh37
NC_000009.10:g.135123323T>G	NCBI36
NG_006669.1:g.19552A>C
NG_006669.2:g.22103A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.254A>C
ENST00000647353.1:n.54-6960A>C
ENST00000651471.1:n.259A>C
ENST00000679909.1:c.28+17050A>C	ENSP00000506089.1:n.28+17050A>C
ENST00000453660.3:n.236A>C
ENST00000538324.2:c.224A>C	ENSP00000483018.1:p.Lys75Thr
ENST00000611156.4:c.224A>C	ENSP00000483265.1:p.Lys75Thr
NM_020469.2:c.224A>C	NP_065202.2:p.Lys75Thr
NM_020469.3:c.224A>C	NP_065202.2:p.Lys75Thr