Canonical Allele Identifier: CA9174551
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs200054594
gnomAD v2: 19-9237226-A-C
gnomAD v4: 19-9126550-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126550A>C , CM000681.2:g.9126550A>C GRCh38
NC_000019.9:g.9237226A>C , CM000681.1:g.9237226A>C GRCh37
NC_000019.8:g.9098226A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.401T>G MANE Select ENSP00000302867.2:p.Val134Gly
NM_001001958.1:c.401T>G MANE Select NP_001001958.1:p.Val134Gly