Canonical Allele Identifier: CA9174517
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs770815327
ExAC: 19:9237065 CG / C
gnomAD v2: 19-9237065-CG-C
gnomAD v3: 19-9126389-CG-C
gnomAD v4: 19-9126389-CG-C
MyVariant Identifiers: chr19:g.9237066del (hg19) chr19:g.9126390del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126390del , CM000681.2:g.9126390del GRCh38
NC_000019.9:g.9237066del , CM000681.1:g.9237066del GRCh37
NC_000019.8:g.9098066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.561del MANE Select ENSP00000302867.2:p.Ala188ProfsTer15
NM_001001958.1:c.561del MANE Select NP_001001958.1:p.Ala188ProfsTer15
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Search 100 bp 3'