Canonical Allele Identifier: CA505453006
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237444G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126768G>A , CM000681.2:g.9126768G>A GRCh38
NC_000019.9:g.9237444G>A , CM000681.1:g.9237444G>A GRCh37
NC_000019.8:g.9098444G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.183C>T MANE Select ENSP00000302867.2:p.Phe61=
NM_001001958.1:c.183C>T MANE Select NP_001001958.1:p.Phe61=