Canonical Allele Identifier: CA403805563
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs2051195847

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214480A>G , CM000681.2:g.9214480A>G GRCh38
NC_000019.9:g.9325156A>G , CM000681.1:g.9325156A>G GRCh37
NC_000019.8:g.9186156A>G NCBI36
NG_027953.1:g.5392T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.358T>C ENSP00000493404.1:p.Tyr120His
ENST00000641669.1:c.358T>C MANE Select ENSP00000493383.1:p.Tyr120His
ENST00000308682.3:c.358T>C ENSP00000310488.2:p.Tyr120His
NM_001005191.2:c.358T>C NP_001005191.1:p.Tyr120His
NM_001005191.3:c.358T>C MANE Select NP_001005191.1:p.Tyr120His