Canonical Allele Identifier: CA403787989
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs2050510540
gnomAD v3: 19-9126521-G-T
gnomAD v4: 19-9126521-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126521G>T , CM000681.2:g.9126521G>T GRCh38
NC_000019.9:g.9237197G>T , CM000681.1:g.9237197G>T GRCh37
NC_000019.8:g.9098197G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.430C>A MANE Select ENSP00000302867.2:p.Leu144Met
NM_001001958.1:c.430C>A MANE Select NP_001001958.1:p.Leu144Met