Canonical Allele Identifier: CA505452708
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9236970T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126294T>A , CM000681.2:g.9126294T>A GRCh38
NC_000019.9:g.9236970T>A , CM000681.1:g.9236970T>A GRCh37
NC_000019.8:g.9097970T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.657A>T MANE Select ENSP00000302867.2:p.Thr219=
NM_001001958.1:c.657A>T MANE Select NP_001001958.1:p.Thr219=
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