Canonical Allele Identifier: CA474413034
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55579191T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811715T>G , CM000673.2:g.55811715T>G GRCh38
NC_000011.9:g.55579191T>G , CM000673.1:g.55579191T>G GRCh37
NC_000011.8:g.55335767T>G NCBI36
NG_052620.1:g.5349T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.249T>G MANE Select ENSP00000485319.1:p.Ala83=
ENST00000333973.3:c.249T>G ENSP00000335529.2:p.Ala83=
ENST00000623450.1:c.249T>G ENSP00000485509.1:p.Ala83=
ENST00000625203.1:c.249T>G ENSP00000485319.1:p.Ala83=
NM_001004738.1:c.249T>G NP_001004738.1:p.Ala83=
NM_001004738.2:c.249T>G MANE Select NP_001004738.1:p.Ala83=