Canonical Allele Identifier: CA276905092

Gene: OR1F1

Linked Data

• dbSNP Id: rs532042317
• gnomAD v2: 16-3253146-C-T
• gnomAD v3: 16-3203146-C-T
• gnomAD v4: 16-3203146-C-T
• MyVariant Identifiers: chr16:g.3253146C>T (hg19) ; chr16:g.3203146C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3203146C>T , CM000678.2:g.3203146C>T	GRCh38
NC_000016.9:g.3253146C>T , CM000678.1:g.3253146C>T	GRCh37
NC_000016.8:g.3193147C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000304646.3:c.-12-1089C>T MANE Select	ENSP00000305424.2:n.-12-1089C>T
ENST00000576468.1:n.418+11809C>T
ENST00000652759.1:n.424-2195C>T
XM_011522506.1:c.19-1089C>T	XP_011520808.1:n.19-1089C>T
XM_011522507.1:c.-12-1089C>T	XP_011520809.1:n.-12-1089C>T
XM_011522508.1:c.-12-1089C>T	XP_011520810.1:n.-12-1089C>T
XM_011522509.1:c.-333C>T	XP_011520811.1:n.-333C>T
XM_011522506.3:c.19-1089C>T	XP_011520808.1:n.19-1089C>T
XM_011522507.3:c.-12-1089C>T	XP_011520809.1:n.-12-1089C>T
NM_001370639.1:c.19-1089C>T	NP_001357568.1:n.19-1089C>T
NM_001370640.2:c.19-1089C>T	NP_001357569.1:n.19-1089C>T
NM_001370641.1:c.-252-81C>T	NP_001357570.1:n.-252-81C>T
NM_012360.2:c.-12-1089C>T	NP_036492.1:n.-12-1089C>T
NM_001370640.3:c.19-1089C>T	NP_001357569.1:n.19-1089C>T