Canonical Allele Identifier: CA380468586
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1315439563
gnomAD v2: 11-55579006-G-A
gnomAD v4: 11-55811530-G-A
MyVariant Identifiers: chr11:g.55579006G>A (hg19) chr11:g.55811530G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811530G>A , CM000673.2:g.55811530G>A GRCh38
NC_000011.9:g.55579006G>A , CM000673.1:g.55579006G>A GRCh37
NC_000011.8:g.55335582G>A NCBI36
NG_052620.1:g.5164G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.64G>A MANE Select ENSP00000485319.1:p.Glu22Lys
ENST00000333973.3:c.64G>A ENSP00000335529.2:p.Glu22Lys
ENST00000623450.1:c.64G>A ENSP00000485509.1:p.Glu22Lys
ENST00000625203.1:c.64G>A ENSP00000485319.1:p.Glu22Lys
NM_001004738.1:c.64G>A NP_001004738.1:p.Glu22Lys
NM_001004738.2:c.64G>A MANE Select NP_001004738.1:p.Glu22Lys
Search 100 bp 5'
Search 100 bp 3'