Canonical Allele Identifier: CA474412729
Gene: OR5L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.55578969G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811493G>T , CM000673.2:g.55811493G>T GRCh38
NC_000011.9:g.55578969G>T , CM000673.1:g.55578969G>T GRCh37
NC_000011.8:g.55335545G>T NCBI36
NG_052620.1:g.5127G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.27G>T MANE Select ENSP00000485319.1:p.Val9=
ENST00000333973.3:c.27G>T ENSP00000335529.2:p.Val9=
ENST00000623450.1:c.27G>T ENSP00000485509.1:p.Val9=
ENST00000625203.1:c.27G>T ENSP00000485319.1:p.Val9=
NM_001004738.1:c.27G>T NP_001004738.1:p.Val9=
NM_001004738.2:c.27G>T MANE Select NP_001004738.1:p.Val9=