Canonical Allele Identifier: CA1882585017
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261608A= , CM000671.2:g.133261608A= GRCh38
NC_000009.11:g.136137011A= , CM000671.1:g.136137011A= GRCh37
NC_000009.10:g.135126832A= NCBI36
NG_006669.1:g.16042T=
NG_006669.2:g.18607T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.129-234T=
ENST00000647353.1:n.54-10456T=
ENST00000651471.1:n.134-234T=
ENST00000679909.1:c.28+13554T= ENSP00000506089.1:n.28+13554T=
ENST00000453660.3:n.111-234T=
ENST00000538324.2:c.99-234T= ENSP00000483018.1:n.99-234T=
ENST00000611156.4:c.99-234T= ENSP00000483265.1:n.99-234T=
NM_020469.2:c.99-234T= NP_065202.2:n.99-234T=
NM_020469.3:c.99-234T= NP_065202.2:n.99-234T=
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