Canonical Allele Identifier: CA474412788
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1853687380
gnomAD v3: 11-55811520-A-G
gnomAD v4: 11-55811520-A-G
MyVariant Identifiers: chr11:g.55578996A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811520A>G , CM000673.2:g.55811520A>G GRCh38
NC_000011.9:g.55578996A>G , CM000673.1:g.55578996A>G GRCh37
NC_000011.8:g.55335572A>G NCBI36
NG_052620.1:g.5154A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.54A>G MANE Select ENSP00000485319.1:p.Ser18=
ENST00000333973.3:c.54A>G ENSP00000335529.2:p.Ser18=
ENST00000623450.1:c.54A>G ENSP00000485509.1:p.Ser18=
ENST00000625203.1:c.54A>G ENSP00000485319.1:p.Ser18=
NM_001004738.1:c.54A>G NP_001004738.1:p.Ser18=
NM_001004738.2:c.54A>G MANE Select NP_001004738.1:p.Ser18=
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