Canonical Allele Identifier: CA631707321
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1397027836
gnomAD v2: 19-9237088-TC-T
gnomAD v3: 19-9126412-TC-T
gnomAD v4: 19-9126412-TC-T
MyVariant Identifiers: chr19:g.9237089del (hg19) chr19:g.9126413del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126413del , CM000681.2:g.9126413del GRCh38
NC_000019.9:g.9237089del , CM000681.1:g.9237089del GRCh37
NC_000019.8:g.9098089del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.538del MANE Select ENSP00000302867.2:p.Glu180AsnfsTer2
NM_001001958.1:c.538del MANE Select NP_001001958.1:p.Glu180AsnfsTer2
Search 100 bp 5'
Search 100 bp 3'