Canonical Allele Identifier: CA505453033
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237075A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126399A>T , CM000681.2:g.9126399A>T GRCh38
NC_000019.9:g.9237075A>T , CM000681.1:g.9237075A>T GRCh37
NC_000019.8:g.9098075A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.552T>A MANE Select ENSP00000302867.2:p.Ile184=
NM_001001958.1:c.552T>A MANE Select NP_001001958.1:p.Ile184=