Canonical Allele Identifier: CA9174499
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs765037122
ExAC: 19:9236975 A / C
gnomAD v2: 19-9236975-A-C
gnomAD v4: 19-9126299-A-C
MyVariant Identifiers: chr19:g.9236975A>C (hg19) chr19:g.9126299A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126299A>C , CM000681.2:g.9126299A>C GRCh38
NC_000019.9:g.9236975A>C , CM000681.1:g.9236975A>C GRCh37
NC_000019.8:g.9097975A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.652T>G MANE Select ENSP00000302867.2:p.Tyr218Asp
NM_001001958.1:c.652T>G MANE Select NP_001001958.1:p.Tyr218Asp
Search 100 bp 5'
Search 100 bp 3'