ClinGen Allele Registry
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Canonical Allele Identifier:
CA375683448
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131097A>G (hg19)
chr9:g.133255710A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255710A>G , CM000671.2:g.133255710A>G
GRCh38
NC_000009.11:g.136131097A>G , CM000671.1:g.136131097A>G
GRCh37
NC_000009.10:g.135120918A>G
NCBI36
NG_006669.1:g.21958T>C
NG_006669.2:g.24506T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.1050T>C
ENST00000647353.1:n.54-4558T>C
ENST00000679909.1:c.28+19452T>C
ENSP00000506089.1:n.28+19452T>C
ENST00000453660.3:n.1032T>C
ENST00000538324.2:c.1018T>C
ENSP00000483018.1:p.Phe340Leu
ENST00000611156.4:c.1018T>C
ENSP00000483265.1:p.Phe340Leu
NM_020469.2:c.1021T>C
NP_065202.2:p.Phe341Leu
NM_020469.3:c.1021T>C
NP_065202.2:p.Phe341Leu
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