Canonical Allele Identifier: CA1882580329
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256097C= , CM000671.2:g.133256097C= GRCh38
NC_000009.11:g.136131484C= , CM000671.1:g.136131484C= GRCh37
NC_000009.10:g.135121305C= NCBI36
NG_006669.1:g.21571G=
NG_006669.2:g.24119G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.663G=
ENST00000647353.1:n.54-4945G=
ENST00000679909.1:c.28+19065G= ENSP00000506089.1:n.28+19065G=
ENST00000453660.3:n.645G=
ENST00000538324.2:c.631G= ENSP00000483018.1:p.Val211=
ENST00000611156.4:c.631G= ENSP00000483265.1:p.Val211=
NM_020469.2:c.634G= NP_065202.2:p.Val212=
NM_020469.3:c.634G= NP_065202.2:p.Val212=