Canonical Allele Identifier: CA380469348
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55579127T>A (hg19) chr11:g.55811651T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811651T>A , CM000673.2:g.55811651T>A GRCh38
NC_000011.9:g.55579127T>A , CM000673.1:g.55579127T>A GRCh37
NC_000011.8:g.55335703T>A NCBI36
NG_052620.1:g.5285T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.185T>A MANE Select ENSP00000485319.1:p.Phe62Tyr
ENST00000333973.3:c.185T>A ENSP00000335529.2:p.Phe62Tyr
ENST00000623450.1:c.185T>A ENSP00000485509.1:p.Phe62Tyr
ENST00000625203.1:c.185T>A ENSP00000485319.1:p.Phe62Tyr
NM_001004738.1:c.185T>A NP_001004738.1:p.Phe62Tyr
NM_001004738.2:c.185T>A MANE Select NP_001004738.1:p.Phe62Tyr
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