Canonical Allele Identifier: CA1882578936
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255532G= , CM000671.2:g.133255532G= GRCh38
NC_000009.11:g.136130919G= , CM000671.1:g.136130919G= GRCh37
NC_000009.10:g.135120740G= NCBI36
NG_006669.1:g.22136C=
NG_006669.2:g.24684C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1228C=
ENST00000647353.1:n.54-4380C=
ENST00000679909.1:c.28+19630C= ENSP00000506089.1:n.28+19630C=
ENST00000453660.3:n.1210C=
ENST00000611156.4:c.*134C= ENSP00000483265.1:n.*134C=
NM_020469.2:c.*134C= NP_065202.2:n.*134C=
NM_020469.3:c.*134C= NP_065202.2:n.*134C=