Canonical Allele Identifier: CA380468685
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs2134455742
gnomAD v3: 11-55811557-T-C
MyVariant Identifiers: chr11:g.55579033T>C (hg19) chr11:g.55811557T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811557T>C , CM000673.2:g.55811557T>C GRCh38
NC_000011.9:g.55579033T>C , CM000673.1:g.55579033T>C GRCh37
NC_000011.8:g.55335609T>C NCBI36
NG_052620.1:g.5191T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.91T>C MANE Select ENSP00000485319.1:p.Phe31Leu
ENST00000333973.3:c.91T>C ENSP00000335529.2:p.Phe31Leu
ENST00000623450.1:c.91T>C ENSP00000485509.1:p.Phe31Leu
ENST00000625203.1:c.91T>C ENSP00000485319.1:p.Phe31Leu
NM_001004738.1:c.91T>C NP_001004738.1:p.Phe31Leu
NM_001004738.2:c.91T>C MANE Select NP_001004738.1:p.Phe31Leu
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