Canonical Allele Identifier: CA9174587
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs765341328
ExAC: 19:9237457 GT / G
gnomAD v2: 19-9237457-GT-G
gnomAD v3: 19-9126781-GT-G
gnomAD v4: 19-9126781-GT-G
MyVariant Identifiers: chr19:g.9237458del (hg19) chr19:g.9126782del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126782del , CM000681.2:g.9126782del GRCh38
NC_000019.9:g.9237458del , CM000681.1:g.9237458del GRCh37
NC_000019.8:g.9098458del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.169del MANE Select ENSP00000302867.2:p.Thr57ProfsTer27
NM_001001958.1:c.169del MANE Select NP_001001958.1:p.Thr57ProfsTer27
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