Canonical Allele Identifier: CA591309059
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257390G>A , CM000671.2:g.133257390G>A GRCh38
NC_000009.11:g.136132777G>A , CM000671.1:g.136132777G>A GRCh37
NC_000009.10:g.135122598G>A NCBI36
NG_006669.1:g.20278C>T
NG_006669.2:g.22826C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+19C>T
ENST00000647353.1:n.54-6238C>T
ENST00000651471.1:n.329+652C>T
ENST00000679909.1:c.28+17772C>T ENSP00000506089.1:n.28+17772C>T
ENST00000453660.3:n.385+19C>T
ENST00000538324.2:c.371+19C>T ENSP00000483018.1:n.371+19C>T
ENST00000611156.4:c.371+19C>T ENSP00000483265.1:n.371+19C>T
NM_020469.2:c.374+19C>T NP_065202.2:n.374+19C>T
NM_020469.3:c.374+19C>T NP_065202.2:n.374+19C>T