Canonical Allele Identifier: CA403804853
Gene: OR7D4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9325055G>C (hg19) chr19:g.9214379G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9214379G>C , CM000681.2:g.9214379G>C GRCh38
NC_000019.9:g.9325055G>C , CM000681.1:g.9325055G>C GRCh37
NC_000019.8:g.9186055G>C NCBI36
NG_027953.1:g.5493C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000641244.1:c.459C>G ENSP00000493404.1:p.Phe153Leu
ENST00000641669.1:c.459C>G MANE Select ENSP00000493383.1:p.Phe153Leu
ENST00000308682.3:c.459C>G ENSP00000310488.2:p.Phe153Leu
NM_001005191.2:c.459C>G NP_001005191.1:p.Phe153Leu
NM_001005191.3:c.459C>G MANE Select NP_001005191.1:p.Phe153Leu
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