Canonical Allele Identifier: CA380468618
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1347820108
gnomAD v2: 11-55579014-A-C
gnomAD v4: 11-55811538-A-C
MyVariant Identifiers: chr11:g.55579014A>C (hg19) chr11:g.55811538A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811538A>C , CM000673.2:g.55811538A>C GRCh38
NC_000011.9:g.55579014A>C , CM000673.1:g.55579014A>C GRCh37
NC_000011.8:g.55335590A>C NCBI36
NG_052620.1:g.5172A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.72A>C MANE Select ENSP00000485319.1:p.Arg24Ser
ENST00000333973.3:c.72A>C ENSP00000335529.2:p.Arg24Ser
ENST00000623450.1:c.72A>C ENSP00000485509.1:p.Arg24Ser
ENST00000625203.1:c.72A>C ENSP00000485319.1:p.Arg24Ser
NM_001004738.1:c.72A>C NP_001004738.1:p.Arg24Ser
NM_001004738.2:c.72A>C MANE Select NP_001004738.1:p.Arg24Ser
Search 100 bp 5'
Search 100 bp 3'