Canonical Allele Identifier: CA403804644
Gene: OR7D4 HGNC NCBI

Linked Data

dbSNP Id: rs116460228
gnomAD v2: 19-9325018-A-C
gnomAD v4: 19-9214342-A-C
MyVariant Identifiers: chr19:g.9325018A>C (hg19) chr19:g.9214342A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214342A>C , CM000681.2:g.9214342A>C GRCh38
NC_000019.9:g.9325018A>C , CM000681.1:g.9325018A>C GRCh37
NC_000019.8:g.9186018A>C NCBI36
NG_027953.1:g.5530T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.496T>G ENSP00000493404.1:p.Leu166Val
ENST00000641669.1:c.496T>G MANE Select ENSP00000493383.1:p.Leu166Val
ENST00000308682.3:c.496T>G ENSP00000310488.2:p.Leu166Val
NM_001005191.2:c.496T>G NP_001005191.1:p.Leu166Val
NM_001005191.3:c.496T>G MANE Select NP_001005191.1:p.Leu166Val
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