Canonical Allele Identifier: CA474412816
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55579011G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811535G>A , CM000673.2:g.55811535G>A GRCh38
NC_000011.9:g.55579011G>A , CM000673.1:g.55579011G>A GRCh37
NC_000011.8:g.55335587G>A NCBI36
NG_052620.1:g.5169G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.69G>A MANE Select ENSP00000485319.1:p.Leu23=
ENST00000333973.3:c.69G>A ENSP00000335529.2:p.Leu23=
ENST00000623450.1:c.69G>A ENSP00000485509.1:p.Leu23=
ENST00000625203.1:c.69G>A ENSP00000485319.1:p.Leu23=
NM_001004738.1:c.69G>A NP_001004738.1:p.Leu23=
NM_001004738.2:c.69G>A MANE Select NP_001004738.1:p.Leu23=
Search 100 bp 5'
Search 100 bp 3'