Canonical Allele Identifier: CA305051669
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs368505350
gnomAD v3: 19-9126625-C-T
gnomAD v4: 19-9126625-C-T
MyVariant Identifiers: chr19:g.9237301C>T (hg19) chr19:g.9126625C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126625C>T , CM000681.2:g.9126625C>T GRCh38
NC_000019.9:g.9237301C>T , CM000681.1:g.9237301C>T GRCh37
NC_000019.8:g.9098301C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.326G>A MANE Select ENSP00000302867.2:p.Gly109Glu
NM_001001958.1:c.326G>A MANE Select NP_001001958.1:p.Gly109Glu
Search 100 bp 5'
Search 100 bp 3'