Canonical Allele Identifier: CA1882583331
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258265C= , CM000671.2:g.133258265C= GRCh38
NC_000009.11:g.136133656C= , CM000671.1:g.136133656C= GRCh37
NC_000009.10:g.135123477C= NCBI36
NG_006669.1:g.19398G=
NG_006669.2:g.21950G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-133G=
ENST00000647353.1:n.54-7113G=
ENST00000651471.1:n.239-133G=
ENST00000679909.1:c.28+16897G= ENSP00000506089.1:n.28+16897G=
ENST00000453660.3:n.216-133G=
ENST00000538324.2:c.204-133G= ENSP00000483018.1:n.204-133G=
ENST00000611156.4:c.204-133G= ENSP00000483265.1:n.204-133G=
NM_020469.2:c.204-133G= NP_065202.2:n.204-133G=
NM_020469.3:c.204-133G= NP_065202.2:n.204-133G=
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