Canonical Allele Identifier: CA505454946

Gene: OR7D4

Linked Data

• MyVariant Identifiers: chr19:g.9325172T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9214496T>G , CM000681.2:g.9214496T>G	GRCh38
NC_000019.9:g.9325172T>G , CM000681.1:g.9325172T>G	GRCh37
NC_000019.8:g.9186172T>G	NCBI36
NG_027953.1:g.5376A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641244.1:c.342A>C	ENSP00000493404.1:p.Leu114=
ENST00000641669.1:c.342A>C MANE Select	ENSP00000493383.1:p.Leu114=
ENST00000308682.3:c.342A>C	ENSP00000310488.2:p.Leu114=
NM_001005191.2:c.342A>C	NP_001005191.1:p.Leu114=
NM_001005191.3:c.342A>C MANE Select	NP_001005191.1:p.Leu114=