Canonical Allele Identifier: CA474412840
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55579023C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811547C>G , CM000673.2:g.55811547C>G GRCh38
NC_000011.9:g.55579023C>G , CM000673.1:g.55579023C>G GRCh37
NC_000011.8:g.55335599C>G NCBI36
NG_052620.1:g.5181C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.81C>G MANE Select ENSP00000485319.1:p.Leu27=
ENST00000333973.3:c.81C>G ENSP00000335529.2:p.Leu27=
ENST00000623450.1:c.81C>G ENSP00000485509.1:p.Leu27=
ENST00000625203.1:c.81C>G ENSP00000485319.1:p.Leu27=
NM_001004738.1:c.81C>G NP_001004738.1:p.Leu27=
NM_001004738.2:c.81C>G MANE Select NP_001004738.1:p.Leu27=