Canonical Allele Identifier: CA1882579371
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255728C= , CM000671.2:g.133255728C= GRCh38
NC_000009.11:g.136131115C= , CM000671.1:g.136131115C= GRCh37
NC_000009.10:g.135120936C= NCBI36
NG_006669.1:g.21940G=
NG_006669.2:g.24488G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1032G=
ENST00000647353.1:n.54-4576G=
ENST00000679909.1:c.28+19434G= ENSP00000506089.1:n.28+19434G=
ENST00000453660.3:n.1014G=
ENST00000538324.2:c.1000G= ENSP00000483018.1:p.Val334=
ENST00000611156.4:c.1000G= ENSP00000483265.1:p.Val334=
NM_020469.2:c.1003G= NP_065202.2:p.Val335=
NM_020469.3:c.1003G= NP_065202.2:p.Val335=