Canonical Allele Identifier: CA380468445
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1472703232
gnomAD v2: 11-55578971-C-T
MyVariant Identifiers: chr11:g.55578971C>T (hg19) chr11:g.55811495C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811495C>T , CM000673.2:g.55811495C>T GRCh38
NC_000011.9:g.55578971C>T , CM000673.1:g.55578971C>T GRCh37
NC_000011.8:g.55335547C>T NCBI36
NG_052620.1:g.5129C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.29C>T MANE Select ENSP00000485319.1:p.Ala10Val
ENST00000333973.3:c.29C>T ENSP00000335529.2:p.Ala10Val
ENST00000623450.1:c.29C>T ENSP00000485509.1:p.Ala10Val
ENST00000625203.1:c.29C>T ENSP00000485319.1:p.Ala10Val
NM_001004738.1:c.29C>T NP_001004738.1:p.Ala10Val
NM_001004738.2:c.29C>T MANE Select NP_001004738.1:p.Ala10Val
Search 100 bp 5'
Search 100 bp 3'