Canonical Allele Identifier: CA403804754
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs1447260567
gnomAD v2: 19-9325036-T-C
gnomAD v4: 19-9214360-T-C
MyVariant Identifiers: chr19:g.9325036T>C (hg19) chr19:g.9214360T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214360T>C , CM000681.2:g.9214360T>C GRCh38
NC_000019.9:g.9325036T>C , CM000681.1:g.9325036T>C GRCh37
NC_000019.8:g.9186036T>C NCBI36
NG_027953.1:g.5512A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000641244.1:c.478A>G ENSP00000493404.1:p.Ile160Val
ENST00000641669.1:c.478A>G MANE Select ENSP00000493383.1:p.Ile160Val
ENST00000308682.3:c.478A>G ENSP00000310488.2:p.Ile160Val
NM_001005191.2:c.478A>G NP_001005191.1:p.Ile160Val
NM_001005191.3:c.478A>G MANE Select NP_001005191.1:p.Ile160Val
Search 100 bp 5'
Search 100 bp 3'