Canonical Allele Identifier: CA1882582690
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257724G= , CM000671.2:g.133257724G= GRCh38
NC_000009.11:g.136133111G= , CM000671.1:g.136133111G= GRCh37
NC_000009.10:g.135122932G= NCBI36
NG_006669.1:g.19943C=
NG_006669.2:g.22491C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-182C=
ENST00000647353.1:n.54-6572C=
ENST00000651471.1:n.329+318C=
ENST00000679909.1:c.28+17438C= ENSP00000506089.1:n.28+17438C=
ENST00000453660.3:n.252-182C=
ENST00000538324.2:c.240-182C= ENSP00000483018.1:n.240-182C=
ENST00000611156.4:c.240-182C= ENSP00000483265.1:n.240-182C=
NM_020469.2:c.240-182C= NP_065202.2:n.240-182C=
NM_020469.3:c.240-182C= NP_065202.2:n.240-182C=
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