Canonical Allele Identifier: CA1882582221
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257317C= , CM000671.2:g.133257317C= GRCh38
NC_000009.11:g.136132704C= , CM000671.1:g.136132704C= GRCh37
NC_000009.10:g.135122525C= NCBI36
NG_006669.1:g.20351G=
NG_006669.2:g.22899G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+92G=
ENST00000647353.1:n.54-6165G=
ENST00000651471.1:n.329+725G=
ENST00000679909.1:c.28+17845G= ENSP00000506089.1:n.28+17845G=
ENST00000453660.3:n.385+92G=
ENST00000538324.2:c.371+92G= ENSP00000483018.1:n.371+92G=
ENST00000611156.4:c.371+92G= ENSP00000483265.1:n.371+92G=
NM_020469.2:c.374+92G= NP_065202.2:n.374+92G=
NM_020469.3:c.374+92G= NP_065202.2:n.374+92G=