Canonical Allele Identifier: CA5992623
Gene: OR5L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2290067
ClinVar RCV Id: RCV004143844
dbSNP Id: rs766074311
ExAC: 11:55578988 G / A
gnomAD v2: 11-55578988-G-A
gnomAD v4: 11-55811512-G-A
COSMIC: COSM5935770
MyVariant Identifiers: chr11:g.55578988G>A (hg19) chr11:g.55811512G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811512G>A , CM000673.2:g.55811512G>A GRCh38
NC_000011.9:g.55578988G>A , CM000673.1:g.55578988G>A GRCh37
NC_000011.8:g.55335564G>A NCBI36
NG_052620.1:g.5146G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.46G>A MANE Select ENSP00000485319.1:p.Gly16Arg
ENST00000333973.3:c.46G>A ENSP00000335529.2:p.Gly16Arg
ENST00000623450.1:c.46G>A ENSP00000485509.1:p.Gly16Arg
ENST00000625203.1:c.46G>A ENSP00000485319.1:p.Gly16Arg
NM_001004738.1:c.46G>A NP_001004738.1:p.Gly16Arg
NM_001004738.2:c.46G>A MANE Select NP_001004738.1:p.Gly16Arg
Search 100 bp 5'
Search 100 bp 3'