Canonical Allele Identifier: CA375686523

Gene: ABO

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257409T>A , CM000671.2:g.133257409T>A	GRCh38
NC_000009.11:g.136132796T>A , CM000671.1:g.136132796T>A	GRCh37
NC_000009.10:g.135122617T>A	NCBI36
NG_006669.1:g.20259A>T
NG_006669.2:g.22807A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.403A>T
ENST00000647353.1:n.54-6257A>T
ENST00000651471.1:n.329+633A>T
ENST00000679909.1:c.28+17753A>T	ENSP00000506089.1:n.28+17753A>T
ENST00000453660.3:n.385A>T
ENST00000538324.2:c.371A>T	ENSP00000483018.1:p.Lys124Ile
ENST00000611156.4:c.371A>T	ENSP00000483265.1:p.Lys124Ile
NM_020469.2:c.374A>T	NP_065202.2:p.Lys125Ile
NM_020469.3:c.374A>T	NP_065202.2:p.Lys125Ile