Canonical Allele Identifier: CA1882580568
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256176G= , CM000671.2:g.133256176G= GRCh38
NC_000009.11:g.136131563G= , CM000671.1:g.136131563G= GRCh37
NC_000009.10:g.135121384G= NCBI36
NG_006669.1:g.21492C=
NG_006669.2:g.24040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.584C=
ENST00000647353.1:n.54-5024C=
ENST00000651471.1:n.510C=
ENST00000679909.1:c.28+18986C= ENSP00000506089.1:n.28+18986C=
ENST00000453660.3:n.566C=
ENST00000538324.2:c.552C= ENSP00000483018.1:p.Ser184=
ENST00000611156.4:c.552C= ENSP00000483265.1:p.Ser184=
NM_020469.2:c.555C= NP_065202.2:p.Ser185=
NM_020469.3:c.555C= NP_065202.2:p.Ser185=