Canonical Allele Identifier: CA690131731
Gene: OR6C64P HGNC NCBI
OR6C70 HGNC NCBI

Linked Data

dbSNP Id: rs1315048663
MyVariant Identifiers: chr12:g.55916785_55916786del (hg19) chr12:g.55523001_55523002del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55523003_55523004del , CM000674.2:g.55523003_55523004del GRCh38
NC_000012.11:g.55916787_55916788del , CM000674.1:g.55916787_55916788del GRCh37
NC_000012.10:g.54203054_54203055del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419708.1:n.411_412del (OR6C64P)
XM_011538339.1:c.-147-29844_-147-29843del (OR6C70) XP_011536641.1:n.-147-29844_-147-29843del...
XM_011538340.1:c.-147-29844_-147-29843del (OR6C70) XP_011536642.1:n.-147-29844_-147-29843del...
XM_011538341.1:c.-147-29844_-147-29843del (OR6C70) XP_011536643.1:n.-147-29844_-147-29843del...
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