Canonical Allele Identifier: CA9175369

Gene: OR7D4

Linked Data

• ClinVar Variation Id: 2381850
• ClinVar RCV Id: RCV004221439
• dbSNP Id: rs147697203
• ExAC: 19:9324916 A / T
• gnomAD v2: 19-9324916-A-T
• gnomAD v3: 19-9214240-A-T
• gnomAD v4: 19-9214240-A-T
• MyVariant Identifiers: chr19:g.9324916A>T (hg19) ; chr19:g.9214240A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9214240A>T , CM000681.2:g.9214240A>T	GRCh38
NC_000019.9:g.9324916A>T , CM000681.1:g.9324916A>T	GRCh37
NC_000019.8:g.9185916A>T	NCBI36
NG_027953.1:g.5632T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641244.1:c.598T>A	ENSP00000493404.1:p.Tyr200Asn
ENST00000641669.1:c.598T>A MANE Select	ENSP00000493383.1:p.Tyr200Asn
ENST00000308682.3:c.598T>A	ENSP00000310488.2:p.Tyr200Asn
NM_001005191.2:c.598T>A	NP_001005191.1:p.Tyr200Asn
NM_001005191.3:c.598T>A MANE Select	NP_001005191.1:p.Tyr200Asn