Canonical Allele Identifier: CA480112876
Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs1416968642
MyVariant Identifiers: chr12:g.55916608A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55522824A>T , CM000674.2:g.55522824A>T GRCh38
NC_000012.11:g.55916608A>T , CM000674.1:g.55916608A>T GRCh37
NC_000012.10:g.54202875A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419708.1:n.232A>T (OR6C64P)
XM_011538339.1:c.-147-29666T>A (OR6C70) XP_011536641.1:n.-147-29666T>A
XM_011538340.1:c.-147-29666T>A (OR6C70) XP_011536642.1:n.-147-29666T>A
XM_011538341.1:c.-147-29666T>A (OR6C70) XP_011536643.1:n.-147-29666T>A