Canonical Allele Identifier: CA1882583375
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258313G= , CM000671.2:g.133258313G= GRCh38
NC_000009.11:g.136133704G= , CM000671.1:g.136133704G= GRCh37
NC_000009.10:g.135123525G= NCBI36
NG_006669.1:g.19350C=
NG_006669.2:g.21902C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-181C=
ENST00000647353.1:n.54-7161C=
ENST00000651471.1:n.239-181C=
ENST00000679909.1:c.28+16849C= ENSP00000506089.1:n.28+16849C=
ENST00000453660.3:n.216-181C=
ENST00000538324.2:c.204-181C= ENSP00000483018.1:n.204-181C=
ENST00000611156.4:c.204-181C= ENSP00000483265.1:n.204-181C=
NM_020469.2:c.204-181C= NP_065202.2:n.204-181C=
NM_020469.3:c.204-181C= NP_065202.2:n.204-181C=
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