Canonical Allele Identifier: CA1882582186
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257259G= , CM000671.2:g.133257259G= GRCh38
NC_000009.11:g.136132646G= , CM000671.1:g.136132646G= GRCh37
NC_000009.10:g.135122467G= NCBI36
NG_006669.1:g.20409C=
NG_006669.2:g.22957C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+150C=
ENST00000647353.1:n.54-6107C=
ENST00000651471.1:n.329+783C=
ENST00000679909.1:c.28+17903C= ENSP00000506089.1:n.28+17903C=
ENST00000453660.3:n.385+150C=
ENST00000538324.2:c.371+150C= ENSP00000483018.1:n.371+150C=
ENST00000611156.4:c.371+150C= ENSP00000483265.1:n.371+150C=
NM_020469.2:c.374+150C= NP_065202.2:n.374+150C=
NM_020469.3:c.374+150C= NP_065202.2:n.374+150C=