Canonical Allele Identifier: CA380468717
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1176551753
gnomAD v2: 11-55579042-A-G
gnomAD v3: 11-55811566-A-G
gnomAD v4: 11-55811566-A-G
MyVariant Identifiers: chr11:g.55579042A>G (hg19) chr11:g.55811566A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811566A>G , CM000673.2:g.55811566A>G GRCh38
NC_000011.9:g.55579042A>G , CM000673.1:g.55579042A>G GRCh37
NC_000011.8:g.55335618A>G NCBI36
NG_052620.1:g.5200A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.100A>G MANE Select ENSP00000485319.1:p.Ile34Val
ENST00000333973.3:c.100A>G ENSP00000335529.2:p.Ile34Val
ENST00000623450.1:c.100A>G ENSP00000485509.1:p.Ile34Val
ENST00000625203.1:c.100A>G ENSP00000485319.1:p.Ile34Val
NM_001004738.1:c.100A>G NP_001004738.1:p.Ile34Val
NM_001004738.2:c.100A>G MANE Select NP_001004738.1:p.Ile34Val
Search 100 bp 5'
Search 100 bp 3'