Canonical Allele Identifier: CA380468939
Gene: OR5L1 HGNC NCBI

Linked Data

gnomAD v4: 11-55811599-A-G
MyVariant Identifiers: chr11:g.55579075A>G (hg19) chr11:g.55811599A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811599A>G , CM000673.2:g.55811599A>G GRCh38
NC_000011.9:g.55579075A>G , CM000673.1:g.55579075A>G GRCh37
NC_000011.8:g.55335651A>G NCBI36
NG_052620.1:g.5233A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.133A>G MANE Select ENSP00000485319.1:p.Met45Val
ENST00000333973.3:c.133A>G ENSP00000335529.2:p.Met45Val
ENST00000623450.1:c.133A>G ENSP00000485509.1:p.Met45Val
ENST00000625203.1:c.133A>G ENSP00000485319.1:p.Met45Val
NM_001004738.1:c.133A>G NP_001004738.1:p.Met45Val
NM_001004738.2:c.133A>G MANE Select NP_001004738.1:p.Met45Val
Search 100 bp 5'
Search 100 bp 3'