Canonical Allele Identifier: CA480116566
Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.55917158C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55523374C>T , CM000674.2:g.55523374C>T GRCh38
NC_000012.11:g.55917158C>T , CM000674.1:g.55917158C>T GRCh37
NC_000012.10:g.54203425C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419708.1:n.782C>T (OR6C64P)
XM_011538339.1:c.-147-30216G>A (OR6C70) XP_011536641.1:n.-147-30216G>A
XM_011538340.1:c.-147-30216G>A (OR6C70) XP_011536642.1:n.-147-30216G>A
XM_011538341.1:c.-147-30216G>A (OR6C70) XP_011536643.1:n.-147-30216G>A