Canonical Allele Identifier: CA474412753
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs2134455682
MyVariant Identifiers: chr11:g.55578984C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811508C>G , CM000673.2:g.55811508C>G GRCh38
NC_000011.9:g.55578984C>G , CM000673.1:g.55578984C>G GRCh37
NC_000011.8:g.55335560C>G NCBI36
NG_052620.1:g.5142C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.42C>G MANE Select ENSP00000485319.1:p.Leu14=
ENST00000333973.3:c.42C>G ENSP00000335529.2:p.Leu14=
ENST00000623450.1:c.42C>G ENSP00000485509.1:p.Leu14=
ENST00000625203.1:c.42C>G ENSP00000485319.1:p.Leu14=
NM_001004738.1:c.42C>G NP_001004738.1:p.Leu14=
NM_001004738.2:c.42C>G MANE Select NP_001004738.1:p.Leu14=