Canonical Allele Identifier: CA1882582189
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257265G= , CM000671.2:g.133257265G= GRCh38
NC_000009.11:g.136132652G= , CM000671.1:g.136132652G= GRCh37
NC_000009.10:g.135122473G= NCBI36
NG_006669.1:g.20403C=
NG_006669.2:g.22951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+144C=
ENST00000647353.1:n.54-6113C=
ENST00000651471.1:n.329+777C=
ENST00000679909.1:c.28+17897C= ENSP00000506089.1:n.28+17897C=
ENST00000453660.3:n.385+144C=
ENST00000538324.2:c.371+144C= ENSP00000483018.1:n.371+144C=
ENST00000611156.4:c.371+144C= ENSP00000483265.1:n.371+144C=
NM_020469.2:c.374+144C= NP_065202.2:n.374+144C=
NM_020469.3:c.374+144C= NP_065202.2:n.374+144C=