Canonical Allele Identifier: CA403786263
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1197516793
gnomAD v2: 19-9236972-T-A
gnomAD v3: 19-9126296-T-A
gnomAD v4: 19-9126296-T-A
MyVariant Identifiers: chr19:g.9236972T>A (hg19) chr19:g.9126296T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126296T>A , CM000681.2:g.9126296T>A GRCh38
NC_000019.9:g.9236972T>A , CM000681.1:g.9236972T>A GRCh37
NC_000019.8:g.9097972T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.655A>T MANE Select ENSP00000302867.2:p.Thr219Ser
NM_001001958.1:c.655A>T MANE Select NP_001001958.1:p.Thr219Ser
Search 100 bp 5'
Search 100 bp 3'