Canonical Allele Identifier: CA9174608
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs10414255
gnomAD v2: 19-9237542-T-C
gnomAD v3: 19-9126866-T-C
gnomAD v4: 19-9126866-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126866T>C , CM000681.2:g.9126866T>C GRCh38
NC_000019.9:g.9237542T>C , CM000681.1:g.9237542T>C GRCh37
NC_000019.8:g.9098542T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.85A>G MANE Select ENSP00000302867.2:p.Met29Val
NM_001001958.1:c.85A>G MANE Select NP_001001958.1:p.Met29Val