Canonical Allele Identifier: CA411817094
Gene: TSPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.43558930C>G (hg19) chr22:g.43162924C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162924C>G , CM000684.2:g.43162924C>G GRCh38
NC_000022.10:g.43558930C>G , CM000684.1:g.43558930C>G GRCh37
NC_000022.9:g.41888874C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.443C>G MANE Select ENSP00000338004.3:p.Thr148Ser
ENST00000329563.8:c.443C>G ENSP00000328973.4:p.Thr148Ser
ENST00000337554.7:c.443C>G ENSP00000338004.3:p.Thr148Ser
ENST00000396265.4:c.443C>G ENSP00000379563.4:p.Thr148Ser
ENST00000583777.5:c.131C>G ENSP00000463495.1:p.Thr44Ser
NM_000714.5:c.443C>G NP_000705.2:p.Thr148Ser
NM_001256530.1:c.443C>G NP_001243459.1:p.Thr148Ser
NM_001256531.1:c.443C>G NP_001243460.1:p.Thr148Ser
NR_046308.1:n.352C>G
NM_000714.6:c.443C>G MANE Select NP_000705.2:p.Thr148Ser
NR_046308.2:n.307C>G
Search 100 bp 5'
Search 100 bp 3'