Canonical Allele Identifier: CA1882582132
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257183G= , CM000671.2:g.133257183G= GRCh38
NC_000009.11:g.136132570G= , CM000671.1:g.136132570G= GRCh37
NC_000009.10:g.135122391G= NCBI36
NG_006669.1:g.20485C=
NG_006669.2:g.23033C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+226C=
ENST00000647353.1:n.54-6031C=
ENST00000651471.1:n.330-827C=
ENST00000679909.1:c.28+17979C= ENSP00000506089.1:n.28+17979C=
ENST00000453660.3:n.385+226C=
ENST00000538324.2:c.371+226C= ENSP00000483018.1:n.371+226C=
ENST00000611156.4:c.371+226C= ENSP00000483265.1:n.371+226C=
NM_020469.2:c.374+226C= NP_065202.2:n.374+226C=
NM_020469.3:c.374+226C= NP_065202.2:n.374+226C=