Canonical Allele Identifier: CA605246657

Gene: OR6C70

Linked Data

• dbSNP Id: rs1161295427
• gnomAD v2: 12-55917215-A-G
• gnomAD v3: 12-55523431-A-G
• gnomAD v4: 12-55523431-A-G
• MyVariant Identifiers: chr12:g.55917215A>G (hg19) ; chr12:g.55523431A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55523431A>G , CM000674.2:g.55523431A>G	GRCh38
NC_000012.11:g.55917215A>G , CM000674.1:g.55917215A>G	GRCh37
NC_000012.10:g.54203482A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538339.1:c.-147-30273T>C	XP_011536641.1:n.-147-30273T>C
XM_011538340.1:c.-147-30273T>C	XP_011536642.1:n.-147-30273T>C
XM_011538341.1:c.-147-30273T>C	XP_011536643.1:n.-147-30273T>C