Canonical Allele Identifier: CA480113662
Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs1873166113
MyVariant Identifiers: chr12:g.55916690T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55522906T>C , CM000674.2:g.55522906T>C GRCh38
NC_000012.11:g.55916690T>C , CM000674.1:g.55916690T>C GRCh37
NC_000012.10:g.54202957T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419708.1:n.314T>C (OR6C64P)
XM_011538339.1:c.-147-29748A>G (OR6C70) XP_011536641.1:n.-147-29748A>G
XM_011538340.1:c.-147-29748A>G (OR6C70) XP_011536642.1:n.-147-29748A>G
XM_011538341.1:c.-147-29748A>G (OR6C70) XP_011536643.1:n.-147-29748A>G