Canonical Allele Identifier: CA9174609
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs760955234
gnomAD v2: 19-9237549-G-C
gnomAD v4: 19-9126873-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126873G>C , CM000681.2:g.9126873G>C GRCh38
NC_000019.9:g.9237549G>C , CM000681.1:g.9237549G>C GRCh37
NC_000019.8:g.9098549G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.78C>G MANE Select ENSP00000302867.2:p.Ile26Met
NM_001001958.1:c.78C>G MANE Select NP_001001958.1:p.Ile26Met