Canonical Allele Identifier: CA480113658
Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs1873166060
MyVariant Identifiers: chr12:g.55916689C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55522905C>T , CM000674.2:g.55522905C>T GRCh38
NC_000012.11:g.55916689C>T , CM000674.1:g.55916689C>T GRCh37
NC_000012.10:g.54202956C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419708.1:n.313C>T (OR6C64P)
XM_011538339.1:c.-147-29747G>A (OR6C70) XP_011536641.1:n.-147-29747G>A
XM_011538340.1:c.-147-29747G>A (OR6C70) XP_011536642.1:n.-147-29747G>A
XM_011538341.1:c.-147-29747G>A (OR6C70) XP_011536643.1:n.-147-29747G>A