Canonical Allele Identifier: CA9174542
Gene: OR7G3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2492698
ClinVar RCV Id: RCV004274335
dbSNP Id: rs373874756
ExAC: 19:9237193 A / T
gnomAD v2: 19-9237193-A-T
gnomAD v3: 19-9126517-A-T
gnomAD v4: 19-9126517-A-T
MyVariant Identifiers: chr19:g.9237193A>T (hg19) chr19:g.9126517A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126517A>T , CM000681.2:g.9126517A>T GRCh38
NC_000019.9:g.9237193A>T , CM000681.1:g.9237193A>T GRCh37
NC_000019.8:g.9098193A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.434T>A MANE Select ENSP00000302867.2:p.Leu145His
NM_001001958.1:c.434T>A MANE Select NP_001001958.1:p.Leu145His
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Search 100 bp 3'