Canonical Allele Identifier: CA380469786
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1164061200

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811723T>C , CM000673.2:g.55811723T>C GRCh38
NC_000011.9:g.55579199T>C , CM000673.1:g.55579199T>C GRCh37
NC_000011.8:g.55335775T>C NCBI36
NG_052620.1:g.5357T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.257T>C MANE Select ENSP00000485319.1:p.Phe86Ser
ENST00000333973.3:c.257T>C ENSP00000335529.2:p.Phe86Ser
ENST00000623450.1:c.257T>C ENSP00000485509.1:p.Phe86Ser
ENST00000625203.1:c.257T>C ENSP00000485319.1:p.Phe86Ser
NM_001004738.1:c.257T>C NP_001004738.1:p.Phe86Ser
NM_001004738.2:c.257T>C MANE Select NP_001004738.1:p.Phe86Ser