Canonical Allele Identifier: CA9174585
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs750146830
gnomAD v2: 19-9237450-C-T
gnomAD v4: 19-9126774-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126774C>T , CM000681.2:g.9126774C>T GRCh38
NC_000019.9:g.9237450C>T , CM000681.1:g.9237450C>T GRCh37
NC_000019.8:g.9098450C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.177G>A MANE Select ENSP00000302867.2:p.Met59Ile
NM_001001958.1:c.177G>A MANE Select NP_001001958.1:p.Met59Ile