Canonical Allele Identifier: CA9175416
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs5020278

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.398C>G ENSP00000493404.1:p.Thr133Arg
ENST00000641669.1:c.398C>G MANE Select ENSP00000493383.1:p.Thr133Arg
ENST00000308682.3:c.398C>G ENSP00000310488.2:p.Thr133Arg
NM_001005191.2:c.398C>G NP_001005191.1:p.Thr133Arg
NM_001005191.3:c.398C>G MANE Select NP_001005191.1:p.Thr133Arg