Canonical Allele Identifier: CA514828424

Gene: TSPO

Linked Data

• dbSNP Id: rs1931496568
• gnomAD v4: 22-43162943-A-G
• MyVariant Identifiers: chr22:g.43558949A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.43162943A>G , CM000684.2:g.43162943A>G	GRCh38
NC_000022.10:g.43558949A>G , CM000684.1:g.43558949A>G	GRCh37
NC_000022.9:g.41888893A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337554.8:c.462A>G MANE Select	ENSP00000338004.3:p.Val154=
ENST00000329563.8:c.462A>G	ENSP00000328973.4:p.Val154=
ENST00000337554.7:c.462A>G	ENSP00000338004.3:p.Val154=
ENST00000396265.4:c.462A>G	ENSP00000379563.4:p.Val154=
ENST00000583777.5:c.150A>G	ENSP00000463495.1:p.Val50=
NM_000714.5:c.462A>G	NP_000705.2:p.Val154=
NM_001256530.1:c.462A>G	NP_001243459.1:p.Val154=
NM_001256531.1:c.462A>G	NP_001243460.1:p.Val154=
NR_046308.1:n.371A>G
NM_000714.6:c.462A>G MANE Select	NP_000705.2:p.Val154=
NR_046308.2:n.326A>G