Canonical Allele Identifier: CA1882582715
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257741C= , CM000671.2:g.133257741C= GRCh38
NC_000009.11:g.136133128C= , CM000671.1:g.136133128C= GRCh37
NC_000009.10:g.135122949C= NCBI36
NG_006669.1:g.19926G=
NG_006669.2:g.22474G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-199G=
ENST00000647353.1:n.54-6589G=
ENST00000651471.1:n.329+301G=
ENST00000679909.1:c.28+17421G= ENSP00000506089.1:n.28+17421G=
ENST00000453660.3:n.252-199G=
ENST00000538324.2:c.240-199G= ENSP00000483018.1:n.240-199G=
ENST00000611156.4:c.240-199G= ENSP00000483265.1:n.240-199G=
NM_020469.2:c.240-199G= NP_065202.2:n.240-199G=
NM_020469.3:c.240-199G= NP_065202.2:n.240-199G=
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