ClinGen Allele Registry
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Canonical Allele Identifier:
CA13531998
Gene: OR2AH1P
HGNC
NCBI
Linked Data
dbSNP Id:
rs11228718
gnomAD v2:
11-56440129-C-T
gnomAD v3:
11-56672653-C-T
gnomAD v4:
11-56672653-C-T
MyVariant Identifiers:
chr11:g.56440129C>T (hg19)
chr11:g.56672653C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.56672653C>T , CM000673.2:g.56672653C>T
GRCh38
NC_000011.9:g.56440129C>T , CM000673.1:g.56440129C>T
GRCh37
NC_000011.8:g.56196705C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000641232.1:n.180-1233G>A
Search 100 bp 5'
Search 100 bp 3'