Canonical Allele Identifier: CA1882582892
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257935A= , CM000671.2:g.133257935A= GRCh38
NC_000009.11:g.136133322A= , CM000671.1:g.136133322A= GRCh37
NC_000009.10:g.135123143A= NCBI36
NG_006669.1:g.19732T=
NG_006669.2:g.22280T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+162T=
ENST00000647353.1:n.54-6783T=
ENST00000651471.1:n.329+107T=
ENST00000679909.1:c.28+17227T= ENSP00000506089.1:n.28+17227T=
ENST00000453660.3:n.251+162T=
ENST00000538324.2:c.239+162T= ENSP00000483018.1:n.239+162T=
ENST00000611156.4:c.239+162T= ENSP00000483265.1:n.239+162T=
NM_020469.2:c.239+162T= NP_065202.2:n.239+162T=
NM_020469.3:c.239+162T= NP_065202.2:n.239+162T=
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