Canonical Allele Identifier: CA474412777
Gene: OR5L1 HGNC NCBI

Linked Data

gnomAD v4: 11-55811568-C-T
MyVariant Identifiers: chr11:g.55579044C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811568C>T , CM000673.2:g.55811568C>T GRCh38
NC_000011.9:g.55579044C>T , CM000673.1:g.55579044C>T GRCh37
NC_000011.8:g.55335620C>T NCBI36
NG_052620.1:g.5202C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.102C>T MANE Select ENSP00000485319.1:p.Ile34=
ENST00000333973.3:c.102C>T ENSP00000335529.2:p.Ile34=
ENST00000623450.1:c.102C>T ENSP00000485509.1:p.Ile34=
ENST00000625203.1:c.102C>T ENSP00000485319.1:p.Ile34=
NM_001004738.1:c.102C>T NP_001004738.1:p.Ile34=
NM_001004738.2:c.102C>T MANE Select NP_001004738.1:p.Ile34=
Search 100 bp 5'
Search 100 bp 3'