Canonical Allele Identifier: CA505452677
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1847665940
COSMIC: COSM715104
MyVariant Identifiers: chr19:g.9236952G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126276G>A , CM000681.2:g.9126276G>A GRCh38
NC_000019.9:g.9236952G>A , CM000681.1:g.9236952G>A GRCh37
NC_000019.8:g.9097952G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.675C>T MANE Select ENSP00000302867.2:p.Val225=
NM_001001958.1:c.675C>T MANE Select NP_001001958.1:p.Val225=