Canonical Allele Identifier: CA1882583001
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258066G= , CM000671.2:g.133258066G= GRCh38
NC_000009.11:g.136133456G= , CM000671.1:g.136133456G= GRCh37
NC_000009.10:g.135123277G= NCBI36
NG_006669.1:g.19598C=
NG_006669.2:g.22149C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+31C=
ENST00000647353.1:n.54-6914C=
ENST00000651471.1:n.305C=
ENST00000679909.1:c.28+17096C= ENSP00000506089.1:n.28+17096C=
ENST00000453660.3:n.251+31C=
ENST00000538324.2:c.239+31C= ENSP00000483018.1:n.239+31C=
ENST00000611156.4:c.239+31C= ENSP00000483265.1:n.239+31C=
NM_020469.2:c.239+31C= NP_065202.2:n.239+31C=
NM_020469.3:c.239+31C= NP_065202.2:n.239+31C=
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