Canonical Allele Identifier: CA9174525
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs776598629
ExAC: 19:9237100 T / TG
gnomAD v2: 19-9237100-T-TG
gnomAD v3: 19-9126424-T-TG
gnomAD v4: 19-9126424-T-TG
MyVariant Identifiers: chr19:g.9237100_9237101insG (hg19) chr19:g.9126424_9126425insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126428dup , CM000681.2:g.9126428dup GRCh38
NC_000019.9:g.9237104dup , CM000681.1:g.9237104dup GRCh37
NC_000019.8:g.9098104dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.526dup MANE Select ENSP00000302867.2:p.His176ProfsTer5
NM_001001958.1:c.526dup MANE Select NP_001001958.1:p.His176ProfsTer5
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