Canonical Allele Identifier: CA9175415
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs5020278

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214440G>A , CM000681.2:g.9214440G>A GRCh38
NC_000019.9:g.9325116G>A , CM000681.1:g.9325116G>A GRCh37
NC_000019.8:g.9186116G>A NCBI36
NG_027953.1:g.5432C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.398C>T ENSP00000493404.1:p.Thr133Met
ENST00000641669.1:c.398C>T MANE Select ENSP00000493383.1:p.Thr133Met
ENST00000308682.3:c.398C>T ENSP00000310488.2:p.Thr133Met
NM_001005191.2:c.398C>T NP_001005191.1:p.Thr133Met
NM_001005191.3:c.398C>T MANE Select NP_001005191.1:p.Thr133Met