ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686702
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136132879C>G (hg19)
chr9:g.133257492C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133257492C>G , CM000671.2:g.133257492C>G
GRCh38
NC_000009.11:g.136132879C>G , CM000671.1:g.136132879C>G
GRCh37
NC_000009.10:g.135122700C>G
NCBI36
NG_006669.1:g.20176G>C
NG_006669.2:g.22724G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.320G>C
ENST00000647353.1:n.54-6340G>C
ENST00000651471.1:n.329+550G>C
ENST00000679909.1:c.28+17670G>C
ENSP00000506089.1:n.28+17670G>C
ENST00000453660.3:n.302G>C
ENST00000538324.2:c.288G>C
ENSP00000483018.1:p.Glu96Asp
ENST00000611156.4:c.288G>C
ENSP00000483265.1:p.Glu96Asp
NM_020469.2:c.291G>C
NP_065202.2:p.Glu97Asp
NM_020469.3:c.291G>C
NP_065202.2:p.Glu97Asp
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