Canonical Allele Identifier: CA403791343
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1253520135
gnomAD v3: 19-9126883-A-T
gnomAD v4: 19-9126883-A-T
COSMIC: COSM369663

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126883A>T , CM000681.2:g.9126883A>T GRCh38
NC_000019.9:g.9237559A>T , CM000681.1:g.9237559A>T GRCh37
NC_000019.8:g.9098559A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.68T>A MANE Select ENSP00000302867.2:p.Leu23Gln
NM_001001958.1:c.68T>A MANE Select NP_001001958.1:p.Leu23Gln