Canonical Allele Identifier: CA1623459441
Gene: TREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41158903C= , CM000668.2:g.41158903C= GRCh38
NC_000006.11:g.41126641C= , CM000668.1:g.41126641C= GRCh37
NC_000006.10:g.41234619C= NCBI36
NG_011561.1:g.9282G= , LRG_631:g.9282G=

Transcript Alleles

HGVS Amino-acid change
ENST00000373113.8:c.646G= MANE Select ENSP00000362205.3:p.Asp216=
ENST00000338469.3:c.483-123G= ENSP00000342651.4:n.483-123G=
ENST00000373113.7:c.646G= ENSP00000362205.3:p.Asp216=
ENST00000373122.8:c.*17G= ENSP00000362214.4:n.*17G=
NM_001271821.1:c.483-123G= NP_001258750.1:n.483-123G=
NM_018965.3:c.646G= , LRG_631t1:c.646G= NP_061838.1:p.Asp216=
XM_006715116.2:c.385G= XP_006715179.1:p.Asp129=
XR_926795.1:n.222+3340C=
XR_926796.1:n.214+3340C=
XR_926797.1:n.188+3340C=
XR_926795.2:n.517+3340C=
XR_926797.2:n.232+3340C=
NM_001271821.2:c.483-123G= NP_001258750.1:n.483-123G=
NM_018965.4:c.646G= MANE Select NP_061838.1:p.Asp216=