Canonical Allele Identifier: CA1882582171
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257233C= , CM000671.2:g.133257233C= GRCh38
NC_000009.11:g.136132620C= , CM000671.1:g.136132620C= GRCh37
NC_000009.10:g.135122441C= NCBI36
NG_006669.1:g.20435G=
NG_006669.2:g.22983G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+176G=
ENST00000647353.1:n.54-6081G=
ENST00000651471.1:n.329+809G=
ENST00000679909.1:c.28+17929G= ENSP00000506089.1:n.28+17929G=
ENST00000453660.3:n.385+176G=
ENST00000538324.2:c.371+176G= ENSP00000483018.1:n.371+176G=
ENST00000611156.4:c.371+176G= ENSP00000483265.1:n.371+176G=
NM_020469.2:c.374+176G= NP_065202.2:n.374+176G=
NM_020469.3:c.374+176G= NP_065202.2:n.374+176G=