Canonical Allele Identifier: CA2407104265
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs1931512417
gnomAD v4: 22-43163166-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163166T>C , CM000684.2:g.43163166T>C GRCh38
NC_000022.10:g.43559172T>C , CM000684.1:g.43559172T>C GRCh37
NC_000022.9:g.41889116T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*175T>C MANE Select ENSP00000338004.3:n.*175T>C
ENST00000329563.8:c.*175T>C ENSP00000328973.4:n.*175T>C
ENST00000337554.7:c.*175T>C ENSP00000338004.3:n.*175T>C
ENST00000396265.4:c.*175T>C ENSP00000379563.4:n.*175T>C
ENST00000583777.5:c.*175T>C ENSP00000463495.1:n.*175T>C
NM_000714.5:c.*175T>C NP_000705.2:n.*175T>C
NM_001256530.1:c.*175T>C NP_001243459.1:n.*175T>C
NM_001256531.1:c.*175T>C NP_001243460.1:n.*175T>C
NR_046308.1:n.594T>C
NM_000714.6:c.*175T>C MANE Select NP_000705.2:n.*175T>C
NR_046308.2:n.549T>C
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