Canonical Allele Identifier: CA5992622
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs67727364
ExAC: 11:55578987 T / C
gnomAD v2: 11-55578987-T-C
gnomAD v3: 11-55811511-T-C
gnomAD v4: 11-55811511-T-C
MyVariant Identifiers: chr11:g.55578987T>C (hg19) chr11:g.55811511T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811511T>C , CM000673.2:g.55811511T>C GRCh38
NC_000011.9:g.55578987T>C , CM000673.1:g.55578987T>C GRCh37
NC_000011.8:g.55335563T>C NCBI36
NG_052620.1:g.5145T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.45T>C MANE Select ENSP00000485319.1:p.Leu15=
ENST00000333973.3:c.45T>C ENSP00000335529.2:p.Leu15=
ENST00000623450.1:c.45T>C ENSP00000485509.1:p.Leu15=
ENST00000625203.1:c.45T>C ENSP00000485319.1:p.Leu15=
NM_001004738.1:c.45T>C NP_001004738.1:p.Leu15=
NM_001004738.2:c.45T>C MANE Select NP_001004738.1:p.Leu15=
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