Canonical Allele Identifier: CA1882582210
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257304G= , CM000671.2:g.133257304G= GRCh38
NC_000009.11:g.136132691G= , CM000671.1:g.136132691G= GRCh37
NC_000009.10:g.135122512G= NCBI36
NG_006669.1:g.20364C=
NG_006669.2:g.22912C=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+105C=
ENST00000647353.1:n.54-6152C=
ENST00000651471.1:n.329+738C=
ENST00000679909.1:c.28+17858C= ENSP00000506089.1:n.28+17858C=
ENST00000453660.3:n.385+105C=
ENST00000538324.2:c.371+105C= ENSP00000483018.1:n.371+105C=
ENST00000611156.4:c.371+105C= ENSP00000483265.1:n.371+105C=
NM_020469.2:c.374+105C= NP_065202.2:n.374+105C=
NM_020469.3:c.374+105C= NP_065202.2:n.374+105C=