Canonical Allele Identifier: CA474822931
Gene: OR5A1 HGNC NCBI

Linked Data

dbSNP Id: rs1382907905
gnomAD v4: 11-59443627-T-G
MyVariant Identifiers: chr11:g.59211100T>G (hg19) chr11:g.59443627T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.59443627T>G , CM000673.2:g.59443627T>G GRCh38
NC_000011.9:g.59211100T>G , CM000673.1:g.59211100T>G GRCh37
NC_000011.8:g.58967676T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641045.1:c.459T>G MANE Select ENSP00000493195.1:p.Val153=
ENST00000302030.2:c.459T>G ENSP00000303096.2:p.Val153=
NM_001004728.1:c.459T>G NP_001004728.1:p.Val153=
XM_011544810.1:c.459T>G XP_011543112.1:p.Val153=
NM_001004728.2:c.459T>G MANE Select NP_001004728.1:p.Val153=
Search 100 bp 5'
Search 100 bp 3'