Canonical Allele Identifier: CA1882578340
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255290T= , CM000671.2:g.133255290T= GRCh38
NC_000009.11:g.136130677T= , CM000671.1:g.136130677T= GRCh37
NC_000009.10:g.135120498T= NCBI36
NG_006669.1:g.22378A=
NG_006669.2:g.24926A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1470A=
ENST00000647353.1:n.54-4138A=
ENST00000679909.1:c.28+19872A= ENSP00000506089.1:n.28+19872A=
ENST00000453660.3:n.1452A=
ENST00000611156.4:c.*376A= ENSP00000483265.1:n.*376A=
NM_020469.2:c.*376A= NP_065202.2:n.*376A=
NM_020469.3:c.*376A= NP_065202.2:n.*376A=
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