ClinGen Allele Registry
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Canonical Allele Identifier:
CA375684288
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131211C>A (hg19)
chr9:g.133255824C>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255824C>A , CM000671.2:g.133255824C>A
GRCh38
NC_000009.11:g.136131211C>A , CM000671.1:g.136131211C>A
GRCh37
NC_000009.10:g.135121032C>A
NCBI36
NG_006669.1:g.21844G>T
NG_006669.2:g.24392G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.936G>T
ENST00000647353.1:n.54-4672G>T
ENST00000679909.1:c.28+19338G>T
ENSP00000506089.1:n.28+19338G>T
ENST00000453660.3:n.918G>T
ENST00000538324.2:c.904G>T
ENSP00000483018.1:p.Glu302Ter
ENST00000611156.4:c.904G>T
ENSP00000483265.1:p.Glu302Ter
NM_020469.2:c.907G>T
NP_065202.2:p.Glu303Ter
NM_020469.3:c.907G>T
NP_065202.2:p.Glu303Ter
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