Canonical Allele Identifier: CA9175373

Gene: OR7D4

Linked Data

• dbSNP Id: rs377419980
• ExAC: 19:9324917 C / A
• gnomAD v2: 19-9324917-C-A
• gnomAD v3: 19-9214241-C-A
• gnomAD v4: 19-9214241-C-A
• MyVariant Identifiers: chr19:g.9324917C>A (hg19) ; chr19:g.9214241C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9214241C>A , CM000681.2:g.9214241C>A	GRCh38
NC_000019.9:g.9324917C>A , CM000681.1:g.9324917C>A	GRCh37
NC_000019.8:g.9185917C>A	NCBI36
NG_027953.1:g.5631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641244.1:c.597G>T	ENSP00000493404.1:p.Leu199Phe
ENST00000641669.1:c.597G>T MANE Select	ENSP00000493383.1:p.Leu199Phe
ENST00000308682.3:c.597G>T	ENSP00000310488.2:p.Leu199Phe
NM_001005191.2:c.597G>T	NP_001005191.1:p.Leu199Phe
NM_001005191.3:c.597G>T MANE Select	NP_001005191.1:p.Leu199Phe