Canonical Allele Identifier: CA1623461394
Gene: TREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41161277A= , CM000668.2:g.41161277A= GRCh38
NC_000006.11:g.41129015A= , CM000668.1:g.41129015A= GRCh37
NC_000006.10:g.41236993A= NCBI36
NG_011561.1:g.6908T= , LRG_631:g.6908T=

Transcript Alleles

HGVS Amino-acid Change
NM_018965.4:c.377T= MANE Select NP_061838.1:p.Val126=
ENST00000373113.8:c.377T= MANE Select ENSP00000362205.3:p.Val126=
NM_001271821.1:c.377T= NP_001258750.1:p.Val126=
NM_001271821.2:c.377T= NP_001258750.1:p.Val126=
NM_018965.3:c.377T= , LRG_631t1:c.377T= NP_061838.1:p.Val126=
ENST00000338469.3:c.377T= ENSP00000342651.4:p.Val126=
ENST00000373113.7:c.377T= ENSP00000362205.3:p.Val126=
ENST00000373122.8:c.377T= ENSP00000362214.4:p.Val126=
XM_006715116.2:c.131-1395T= XP_006715179.1:n.131-1395T=
XR_926795.1:n.222+5714A=
XR_926795.2:n.517+5714A=
XR_926796.1:n.214+5714A=
XR_926797.1:n.188+5714A=
XR_926797.2:n.232+5714A=