Canonical Allele Identifier: CA2407104181
Gene: TSPO HGNC NCBI

Linked Data

dbSNP Id: rs1931504257
gnomAD v4: 22-43163028-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43163028G>A , CM000684.2:g.43163028G>A GRCh38
NC_000022.10:g.43559034G>A , CM000684.1:g.43559034G>A GRCh37
NC_000022.9:g.41888978G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337554.8:c.*37G>A MANE Select ENSP00000338004.3:n.*37G>A
ENST00000329563.8:c.*37G>A ENSP00000328973.4:n.*37G>A
ENST00000337554.7:c.*37G>A ENSP00000338004.3:n.*37G>A
ENST00000396265.4:c.*37G>A ENSP00000379563.4:n.*37G>A
ENST00000583777.5:c.*37G>A ENSP00000463495.1:n.*37G>A
NM_000714.5:c.*37G>A NP_000705.2:n.*37G>A
NM_001256530.1:c.*37G>A NP_001243459.1:n.*37G>A
NM_001256531.1:c.*37G>A NP_001243460.1:n.*37G>A
NR_046308.1:n.456G>A
NM_000714.6:c.*37G>A MANE Select NP_000705.2:n.*37G>A
NR_046308.2:n.411G>A
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