Canonical Allele Identifier: CA1882582019
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257079C= , CM000671.2:g.133257079C= GRCh38
NC_000009.11:g.136132466C= , CM000671.1:g.136132466C= GRCh37
NC_000009.10:g.135122287C= NCBI36
NG_006669.1:g.20589G=
NG_006669.2:g.23137G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+330G=
ENST00000647353.1:n.54-5927G=
ENST00000651471.1:n.330-723G=
ENST00000679909.1:c.28+18083G= ENSP00000506089.1:n.28+18083G=
ENST00000453660.3:n.385+330G=
ENST00000538324.2:c.371+330G= ENSP00000483018.1:n.371+330G=
ENST00000611156.4:c.371+330G= ENSP00000483265.1:n.371+330G=
NM_020469.2:c.374+330G= NP_065202.2:n.374+330G=
NM_020469.3:c.374+330G= NP_065202.2:n.374+330G=