Canonical Allele Identifier: CA403786301
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9236974T>C (hg19) chr19:g.9126298T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126298T>C , CM000681.2:g.9126298T>C GRCh38
NC_000019.9:g.9236974T>C , CM000681.1:g.9236974T>C GRCh37
NC_000019.8:g.9097974T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.653A>G MANE Select ENSP00000302867.2:p.Tyr218Cys
NM_001001958.1:c.653A>G MANE Select NP_001001958.1:p.Tyr218Cys
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Search 100 bp 3'