Canonical Allele Identifier: CA380469721
Gene: OR5L1 HGNC NCBI

Linked Data

dbSNP Id: rs1339897309
gnomAD v3: 11-55811713-G-C
gnomAD v4: 11-55811713-G-C
MyVariant Identifiers: chr11:g.55579189G>C (hg19) chr11:g.55811713G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.55811713G>C , CM000673.2:g.55811713G>C GRCh38
NC_000011.9:g.55579189G>C , CM000673.1:g.55579189G>C GRCh37
NC_000011.8:g.55335765G>C NCBI36
NG_052620.1:g.5347G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000625203.2:c.247G>C MANE Select ENSP00000485319.1:p.Ala83Pro
ENST00000333973.3:c.247G>C ENSP00000335529.2:p.Ala83Pro
ENST00000623450.1:c.247G>C ENSP00000485509.1:p.Ala83Pro
ENST00000625203.1:c.247G>C ENSP00000485319.1:p.Ala83Pro
NM_001004738.1:c.247G>C NP_001004738.1:p.Ala83Pro
NM_001004738.2:c.247G>C MANE Select NP_001004738.1:p.Ala83Pro
Search 100 bp 5'
Search 100 bp 3'