Canonical Allele Identifier: CA474413462

Gene: OR5L1

Linked Data

• dbSNP Id: rs1853702109
• gnomAD v4: 11-55812042-C-T
• MyVariant Identifiers: chr11:g.55579518C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.55812042C>T , CM000673.2:g.55812042C>T	GRCh38
NC_000011.9:g.55579518C>T , CM000673.1:g.55579518C>T	GRCh37
NC_000011.8:g.55336094C>T	NCBI36
NG_052620.1:g.5676C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625203.2:c.576C>T MANE Select	ENSP00000485319.1:p.Ile192=
ENST00000333973.3:c.576C>T	ENSP00000335529.2:p.Ile192=
ENST00000623450.1:c.576C>T	ENSP00000485509.1:p.Ile192=
ENST00000625203.1:c.576C>T	ENSP00000485319.1:p.Ile192=
NM_001004738.1:c.576C>T	NP_001004738.1:p.Ile192=
NM_001004738.2:c.576C>T MANE Select	NP_001004738.1:p.Ile192=