Canonical Allele Identifier: CA403804927

Gene: OR7D4

Linked Data

• MyVariant Identifiers: chr19:g.9325063T>C (hg19) ; chr19:g.9214387T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9214387T>C , CM000681.2:g.9214387T>C	GRCh38
NC_000019.9:g.9325063T>C , CM000681.1:g.9325063T>C	GRCh37
NC_000019.8:g.9186063T>C	NCBI36
NG_027953.1:g.5485A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641244.1:c.451A>G	ENSP00000493404.1:p.Ile151Val
ENST00000641669.1:c.451A>G MANE Select	ENSP00000493383.1:p.Ile151Val
ENST00000308682.3:c.451A>G	ENSP00000310488.2:p.Ile151Val
NM_001005191.2:c.451A>G	NP_001005191.1:p.Ile151Val
NM_001005191.3:c.451A>G MANE Select	NP_001005191.1:p.Ile151Val