Canonical Allele Identifier: CA403786336
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs2050508781
MyVariant Identifiers: chr19:g.9236977G>C (hg19) chr19:g.9126301G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126301G>C , CM000681.2:g.9126301G>C GRCh38
NC_000019.9:g.9236977G>C , CM000681.1:g.9236977G>C GRCh37
NC_000019.8:g.9097977G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.650C>G MANE Select ENSP00000302867.2:p.Ser217Cys
NM_001001958.1:c.650C>G MANE Select NP_001001958.1:p.Ser217Cys
Search 100 bp 5'
Search 100 bp 3'