Canonical Allele Identifier: CA1882582702
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257733T= , CM000671.2:g.133257733T= GRCh38
NC_000009.11:g.136133120T= , CM000671.1:g.136133120T= GRCh37
NC_000009.10:g.135122941T= NCBI36
NG_006669.1:g.19934A=
NG_006669.2:g.22482A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-191A=
ENST00000647353.1:n.54-6581A=
ENST00000651471.1:n.329+309A=
ENST00000679909.1:c.28+17429A= ENSP00000506089.1:n.28+17429A=
ENST00000453660.3:n.252-191A=
ENST00000538324.2:c.240-191A= ENSP00000483018.1:n.240-191A=
ENST00000611156.4:c.240-191A= ENSP00000483265.1:n.240-191A=
NM_020469.2:c.240-191A= NP_065202.2:n.240-191A=
NM_020469.3:c.240-191A= NP_065202.2:n.240-191A=
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