Canonical Allele Identifier: CA380469204
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs770618559
gnomAD v4: 11-55811636-C-A
MyVariant Identifiers: chr11:g.55579112C>A (hg19) chr11:g.55811636C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811636C>A , CM000673.2:g.55811636C>A GRCh38
NC_000011.9:g.55579112C>A , CM000673.1:g.55579112C>A GRCh37
NC_000011.8:g.55335688C>A NCBI36
NG_052620.1:g.5270C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.170C>A MANE Select ENSP00000485319.1:p.Thr57Asn
ENST00000333973.3:c.170C>A ENSP00000335529.2:p.Thr57Asn
ENST00000623450.1:c.170C>A ENSP00000485509.1:p.Thr57Asn
ENST00000625203.1:c.170C>A ENSP00000485319.1:p.Thr57Asn
NM_001004738.1:c.170C>A NP_001004738.1:p.Thr57Asn
NM_001004738.2:c.170C>A MANE Select NP_001004738.1:p.Thr57Asn
Search 100 bp 5'
Search 100 bp 3'