ClinGen Allele Registry
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Canonical Allele Identifier:
CA375684165
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131198T>C (hg19)
chr9:g.133255811T>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255811T>C , CM000671.2:g.133255811T>C
GRCh38
NC_000009.11:g.136131198T>C , CM000671.1:g.136131198T>C
GRCh37
NC_000009.10:g.135121019T>C
NCBI36
NG_006669.1:g.21857A>G
NG_006669.2:g.24405A>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.949A>G
ENST00000647353.1:n.54-4659A>G
ENST00000679909.1:c.28+19351A>G
ENSP00000506089.1:n.28+19351A>G
ENST00000453660.3:n.931A>G
ENST00000538324.2:c.917A>G
ENSP00000483018.1:p.Asn306Ser
ENST00000611156.4:c.917A>G
ENSP00000483265.1:p.Asn306Ser
NM_020469.2:c.920A>G
NP_065202.2:p.Asn307Ser
NM_020469.3:c.920A>G
NP_065202.2:p.Asn307Ser
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