Canonical Allele Identifier: CA474412878
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55579101T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811625T>G , CM000673.2:g.55811625T>G GRCh38
NC_000011.9:g.55579101T>G , CM000673.1:g.55579101T>G GRCh37
NC_000011.8:g.55335677T>G NCBI36
NG_052620.1:g.5259T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.159T>G MANE Select ENSP00000485319.1:p.Ser53=
ENST00000333973.3:c.159T>G ENSP00000335529.2:p.Ser53=
ENST00000623450.1:c.159T>G ENSP00000485509.1:p.Ser53=
ENST00000625203.1:c.159T>G ENSP00000485319.1:p.Ser53=
NM_001004738.1:c.159T>G NP_001004738.1:p.Ser53=
NM_001004738.2:c.159T>G MANE Select NP_001004738.1:p.Ser53=
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