Canonical Allele Identifier: CA5992703
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs759593107
ExAC: 11:55579295 T / C
gnomAD v2: 11-55579295-T-C
gnomAD v4: 11-55811819-T-C
MyVariant Identifiers: chr11:g.55579295T>C (hg19) chr11:g.55811819T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811819T>C , CM000673.2:g.55811819T>C GRCh38
NC_000011.9:g.55579295T>C , CM000673.1:g.55579295T>C GRCh37
NC_000011.8:g.55335871T>C NCBI36
NG_052620.1:g.5453T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.353T>C MANE Select ENSP00000485319.1:p.Met118Thr
ENST00000333973.3:c.353T>C ENSP00000335529.2:p.Met118Thr
ENST00000623450.1:c.353T>C ENSP00000485509.1:p.Met118Thr
ENST00000625203.1:c.353T>C ENSP00000485319.1:p.Met118Thr
NM_001004738.1:c.353T>C NP_001004738.1:p.Met118Thr
NM_001004738.2:c.353T>C MANE Select NP_001004738.1:p.Met118Thr
Search 100 bp 5'
Search 100 bp 3'