Canonical Allele Identifier: CA631707304
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1315742693
gnomAD v2: 19-9237180-G-GA
gnomAD v4: 19-9126504-G-GA
MyVariant Identifiers: chr19:g.9237180_9237181insA (hg19) chr19:g.9126504_9126505insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126506dup , CM000681.2:g.9126506dup GRCh38
NC_000019.9:g.9237182dup , CM000681.1:g.9237182dup GRCh37
NC_000019.8:g.9098182dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.446dup MANE Select ENSP00000302867.2:p.Ile150HisfsTer3
NM_001001958.1:c.446dup MANE Select NP_001001958.1:p.Ile150HisfsTer3
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