Canonical Allele Identifier: CA505454809

Gene: OR7D4

Linked Data

• MyVariant Identifiers: chr19:g.9325070A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9214394A>T , CM000681.2:g.9214394A>T	GRCh38
NC_000019.9:g.9325070A>T , CM000681.1:g.9325070A>T	GRCh37
NC_000019.8:g.9186070A>T	NCBI36
NG_027953.1:g.5478T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000641244.1:c.444T>A	ENSP00000493404.1:p.Ser148=
ENST00000641669.1:c.444T>A MANE Select	ENSP00000493383.1:p.Ser148=
ENST00000308682.3:c.444T>A	ENSP00000310488.2:p.Ser148=
NM_001005191.2:c.444T>A	NP_001005191.1:p.Ser148=
NM_001005191.3:c.444T>A MANE Select	NP_001005191.1:p.Ser148=