Canonical Allele Identifier: CA9174588
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs531567500
ExAC: 19:9237458 TGTGGAG / T
gnomAD v2: 19-9237458-TGTGGAG-T
gnomAD v3: 19-9126782-TGTGGAG-T
gnomAD v4: 19-9126782-TGTGGAG-T
MyVariant Identifiers: chr19:g.9237459_9237464del (hg19) chr19:g.9126783_9126788del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126787_9126792del , CM000681.2:g.9126787_9126792del GRCh38
NC_000019.9:g.9237463_9237468del , CM000681.1:g.9237463_9237468del GRCh37
NC_000019.8:g.9098463_9098468del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.163_168del MANE Select ENSP00000302867.2:p.Leu55_His56del
NM_001001958.1:c.163_168del MANE Select NP_001001958.1:p.Leu55_His56del
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