ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686134
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131564G>T (hg19)
chr9:g.133256177G>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256177G>T , CM000671.2:g.133256177G>T
GRCh38
NC_000009.11:g.136131564G>T , CM000671.1:g.136131564G>T
GRCh37
NC_000009.10:g.135121385G>T
NCBI36
NG_006669.1:g.21491C>A
NG_006669.2:g.24039C>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.583C>A
ENST00000647353.1:n.54-5025C>A
ENST00000651471.1:n.509C>A
ENST00000679909.1:c.28+18985C>A
ENSP00000506089.1:n.28+18985C>A
ENST00000453660.3:n.565C>A
ENST00000538324.2:c.551C>A
ENSP00000483018.1:p.Ser184Tyr
ENST00000611156.4:c.551C>A
ENSP00000483265.1:p.Ser184Tyr
NM_020469.2:c.554C>A
NP_065202.2:p.Ser185Tyr
NM_020469.3:c.554C>A
NP_065202.2:p.Ser185Tyr
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