Canonical Allele Identifier: CA1882583510
Gene: ABO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258422G= , CM000671.2:g.133258422G= GRCh38
NC_000009.11:g.136133813G= , CM000671.1:g.136133813G= GRCh37
NC_000009.10:g.135123634G= NCBI36
NG_006669.1:g.19241C=
NG_006669.2:g.21793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-290C=
ENST00000647353.1:n.54-7270C=
ENST00000651471.1:n.239-290C=
ENST00000679909.1:c.28+16740C= ENSP00000506089.1:n.28+16740C=
ENST00000453660.3:n.216-290C=
ENST00000538324.2:c.204-290C= ENSP00000483018.1:n.204-290C=
ENST00000611156.4:c.204-290C= ENSP00000483265.1:n.204-290C=
NM_020469.2:c.204-290C= NP_065202.2:n.204-290C=
NM_020469.3:c.204-290C= NP_065202.2:n.204-290C=
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