Canonical Allele Identifier: CA474412786
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55578996A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811520A>C , CM000673.2:g.55811520A>C GRCh38
NC_000011.9:g.55578996A>C , CM000673.1:g.55578996A>C GRCh37
NC_000011.8:g.55335572A>C NCBI36
NG_052620.1:g.5154A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.54A>C MANE Select ENSP00000485319.1:p.Ser18=
ENST00000333973.3:c.54A>C ENSP00000335529.2:p.Ser18=
ENST00000623450.1:c.54A>C ENSP00000485509.1:p.Ser18=
ENST00000625203.1:c.54A>C ENSP00000485319.1:p.Ser18=
NM_001004738.1:c.54A>C NP_001004738.1:p.Ser18=
NM_001004738.2:c.54A>C MANE Select NP_001004738.1:p.Ser18=