Canonical Allele Identifier: CA690131911
Gene: OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs1384186621
gnomAD v3: 12-55523423-G-T
gnomAD v4: 12-55523423-G-T
MyVariant Identifiers: chr12:g.55917207G>T (hg19) chr12:g.55523423G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55523423G>T , CM000674.2:g.55523423G>T GRCh38
NC_000012.11:g.55917207G>T , CM000674.1:g.55917207G>T GRCh37
NC_000012.10:g.54203474G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538339.1:c.-147-30265C>A XP_011536641.1:n.-147-30265C>A
XM_011538340.1:c.-147-30265C>A XP_011536642.1:n.-147-30265C>A
XM_011538341.1:c.-147-30265C>A XP_011536643.1:n.-147-30265C>A
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