Canonical Allele Identifier: CA403786780
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs2050509256
gnomAD v4: 19-9126367-T-C
MyVariant Identifiers: chr19:g.9237043T>C (hg19) chr19:g.9126367T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126367T>C , CM000681.2:g.9126367T>C GRCh38
NC_000019.9:g.9237043T>C , CM000681.1:g.9237043T>C GRCh37
NC_000019.8:g.9098043T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.584A>G MANE Select ENSP00000302867.2:p.Asn195Ser
NM_001001958.1:c.584A>G MANE Select NP_001001958.1:p.Asn195Ser
Search 100 bp 5'
Search 100 bp 3'