ClinGen Allele Registry
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Canonical Allele Identifier:
CA375683583
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131120G>T (hg19)
chr9:g.133255733G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133255733G>T , CM000671.2:g.133255733G>T
GRCh38
NC_000009.11:g.136131120G>T , CM000671.1:g.136131120G>T
GRCh37
NC_000009.10:g.135120941G>T
NCBI36
NG_006669.1:g.21935C>A
NG_006669.2:g.24483C>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000453660.4:n.1027C>A
ENST00000647353.1:n.54-4581C>A
ENST00000679909.1:c.28+19429C>A
ENSP00000506089.1:n.28+19429C>A
ENST00000453660.3:n.1009C>A
ENST00000538324.2:c.995C>A
ENSP00000483018.1:p.Pro332His
ENST00000611156.4:c.995C>A
ENSP00000483265.1:p.Pro332His
NM_020469.2:c.998C>A
NP_065202.2:p.Pro333His
NM_020469.3:c.998C>A
NP_065202.2:p.Pro333His
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