Canonical Allele Identifier: CA2657109466
Gene: TSPO HGNC NCBI

Linked Data

gnomAD v4: 22-43162730-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162730G>A , CM000684.2:g.43162730G>A GRCh38
NC_000022.10:g.43558736G>A , CM000684.1:g.43558736G>A GRCh37
NC_000022.9:g.41888680G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337554.8:c.322-73G>A MANE Select ENSP00000338004.3:n.322-73G>A
ENST00000329563.8:c.322-73G>A ENSP00000328973.4:n.322-73G>A
ENST00000337554.7:c.322-73G>A ENSP00000338004.3:n.322-73G>A
ENST00000396265.4:c.322-73G>A ENSP00000379563.4:n.322-73G>A
ENST00000583777.5:c.10-73G>A ENSP00000463495.1:n.10-73G>A
NM_000714.5:c.322-73G>A NP_000705.2:n.322-73G>A
NM_001256530.1:c.322-73G>A NP_001243459.1:n.322-73G>A
NM_001256531.1:c.322-73G>A NP_001243460.1:n.322-73G>A
NR_046308.1:n.231-73G>A
NM_000714.6:c.322-73G>A MANE Select NP_000705.2:n.322-73G>A
NR_046308.2:n.186-73G>A
Search 100 bp 5'
Search 100 bp 3'