Canonical Allele Identifier: CA1623461361
Gene: TREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41161255C= , CM000668.2:g.41161255C= GRCh38
NC_000006.11:g.41128993C= , CM000668.1:g.41128993C= GRCh37
NC_000006.10:g.41236971C= NCBI36
NG_011561.1:g.6930G= , LRG_631:g.6930G=

Transcript Alleles

HGVS Amino-acid change
ENST00000373113.8:c.391+8G= MANE Select ENSP00000362205.3:n.391+8G=
ENST00000338469.3:c.391+8G= ENSP00000342651.4:n.391+8G=
ENST00000373113.7:c.391+8G= ENSP00000362205.3:n.391+8G=
ENST00000373122.8:c.391+8G= ENSP00000362214.4:n.391+8G=
NM_001271821.1:c.391+8G= NP_001258750.1:n.391+8G=
NM_018965.3:c.391+8G= , LRG_631t1:c.391+8G= NP_061838.1:n.391+8G=
XM_006715116.2:c.131-1373G= XP_006715179.1:n.131-1373G=
XR_926795.1:n.222+5692C=
XR_926796.1:n.214+5692C=
XR_926797.1:n.188+5692C=
XR_926795.2:n.517+5692C=
XR_926797.2:n.232+5692C=
NM_001271821.2:c.391+8G= NP_001258750.1:n.391+8G=
NM_018965.4:c.391+8G= MANE Select NP_061838.1:n.391+8G=