Canonical Allele Identifier: CA403790172
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237452T>A (hg19) chr19:g.9126776T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126776T>A , CM000681.2:g.9126776T>A GRCh38
NC_000019.9:g.9237452T>A , CM000681.1:g.9237452T>A GRCh37
NC_000019.8:g.9098452T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.175A>T MANE Select ENSP00000302867.2:p.Met59Leu
NM_001001958.1:c.175A>T MANE Select NP_001001958.1:p.Met59Leu
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