Canonical Allele Identifier: CA474412841
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1853687848
gnomAD v3: 11-55811547-C-T
gnomAD v4: 11-55811547-C-T
MyVariant Identifiers: chr11:g.55579023C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811547C>T , CM000673.2:g.55811547C>T GRCh38
NC_000011.9:g.55579023C>T , CM000673.1:g.55579023C>T GRCh37
NC_000011.8:g.55335599C>T NCBI36
NG_052620.1:g.5181C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.81C>T MANE Select ENSP00000485319.1:p.Leu27=
ENST00000333973.3:c.81C>T ENSP00000335529.2:p.Leu27=
ENST00000623450.1:c.81C>T ENSP00000485509.1:p.Leu27=
ENST00000625203.1:c.81C>T ENSP00000485319.1:p.Leu27=
NM_001004738.1:c.81C>T NP_001004738.1:p.Leu27=
NM_001004738.2:c.81C>T MANE Select NP_001004738.1:p.Leu27=
Search 100 bp 5'
Search 100 bp 3'