Canonical Allele Identifier: CA403805318
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs2146006849

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214447G>T , CM000681.2:g.9214447G>T GRCh38
NC_000019.9:g.9325123G>T , CM000681.1:g.9325123G>T GRCh37
NC_000019.8:g.9186123G>T NCBI36
NG_027953.1:g.5425C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.391C>A ENSP00000493404.1:p.His131Asn
ENST00000641669.1:c.391C>A MANE Select ENSP00000493383.1:p.His131Asn
ENST00000308682.3:c.391C>A ENSP00000310488.2:p.His131Asn
NM_001005191.2:c.391C>A NP_001005191.1:p.His131Asn
NM_001005191.3:c.391C>A MANE Select NP_001005191.1:p.His131Asn