Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA237544212

Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs185264649

gnomAD v3: 12-55522901-T-C

gnomAD v4: 12-55522901-T-C

MyVariant Identifiers: chr12:g.55916685T>C (hg19) chr12:g.55522901T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55522901T>C , CM000674.2:g.55522901T>C	GRCh38
NC_000012.11:g.55916685T>C , CM000674.1:g.55916685T>C	GRCh37
NC_000012.10:g.54202952T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419708.1:n.309T>C (OR6C64P)
XM_011538339.1:c.-147-29743A>G (OR6C70)	XP_011536641.1:n.-147-29743A>G
XM_011538340.1:c.-147-29743A>G (OR6C70)	XP_011536642.1:n.-147-29743A>G
XM_011538341.1:c.-147-29743A>G (OR6C70)	XP_011536643.1:n.-147-29743A>G

Search 100 bp 5'

Search 100 bp 3'