Canonical Allele Identifier: CA1882582798
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257819G= , CM000671.2:g.133257819G= GRCh38
NC_000009.11:g.136133206G= , CM000671.1:g.136133206G= GRCh37
NC_000009.10:g.135123027G= NCBI36
NG_006669.1:g.19848C=
NG_006669.2:g.22396C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-277C=
ENST00000647353.1:n.54-6667C=
ENST00000651471.1:n.329+223C=
ENST00000679909.1:c.28+17343C= ENSP00000506089.1:n.28+17343C=
ENST00000453660.3:n.252-277C=
ENST00000538324.2:c.240-277C= ENSP00000483018.1:n.240-277C=
ENST00000611156.4:c.240-277C= ENSP00000483265.1:n.240-277C=
NM_020469.2:c.240-277C= NP_065202.2:n.240-277C=
NM_020469.3:c.240-277C= NP_065202.2:n.240-277C=