Canonical Allele Identifier: CA237544317
Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs954891836
gnomAD v3: 12-55523314-C-T
gnomAD v4: 12-55523314-C-T
MyVariant Identifiers: chr12:g.55917098C>T (hg19) chr12:g.55523314C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55523314C>T , CM000674.2:g.55523314C>T GRCh38
NC_000012.11:g.55917098C>T , CM000674.1:g.55917098C>T GRCh37
NC_000012.10:g.54203365C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419708.1:n.722C>T (OR6C64P)
XM_011538339.1:c.-147-30156G>A (OR6C70) XP_011536641.1:n.-147-30156G>A
XM_011538340.1:c.-147-30156G>A (OR6C70) XP_011536642.1:n.-147-30156G>A
XM_011538341.1:c.-147-30156G>A (OR6C70) XP_011536643.1:n.-147-30156G>A
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