Canonical Allele Identifier: CA1623461644
Gene: TREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41161480G= , CM000668.2:g.41161480G= GRCh38
NC_000006.11:g.41129218G= , CM000668.1:g.41129218G= GRCh37
NC_000006.10:g.41237196G= NCBI36
NG_011561.1:g.6705C= , LRG_631:g.6705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373113.8:c.174C= MANE Select ENSP00000362205.3:p.Gly58=
ENST00000338469.3:c.174C= ENSP00000342651.4:p.Gly58=
ENST00000373113.7:c.174C= ENSP00000362205.3:p.Gly58=
ENST00000373122.8:c.174C= ENSP00000362214.4:p.Gly58=
NM_001271821.1:c.174C= NP_001258750.1:p.Gly58=
NM_018965.3:c.174C= , LRG_631t1:c.174C= NP_061838.1:p.Gly58=
XM_006715116.2:c.130+1563C= XP_006715179.1:n.130+1563C=
XR_926795.1:n.222+5917G=
XR_926796.1:n.214+5917G=
XR_926797.1:n.188+5917G=
XR_926795.2:n.517+5917G=
XR_926797.2:n.232+5917G=
NM_001271821.2:c.174C= NP_001258750.1:p.Gly58=
NM_018965.4:c.174C= MANE Select NP_061838.1:p.Gly58=