Canonical Allele Identifier: CA1623461633
Gene: TREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41161469C= , CM000668.2:g.41161469C= GRCh38
NC_000006.11:g.41129207C= , CM000668.1:g.41129207C= GRCh37
NC_000006.10:g.41237185C= NCBI36
NG_011561.1:g.6716G= , LRG_631:g.6716G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373113.8:c.185G= MANE Select ENSP00000362205.3:p.Arg62=
ENST00000338469.3:c.185G= ENSP00000342651.4:p.Arg62=
ENST00000373113.7:c.185G= ENSP00000362205.3:p.Arg62=
ENST00000373122.8:c.185G= ENSP00000362214.4:p.Arg62=
NM_001271821.1:c.185G= NP_001258750.1:p.Arg62=
NM_018965.3:c.185G= , LRG_631t1:c.185G= NP_061838.1:p.Arg62=
XM_006715116.2:c.130+1574G= XP_006715179.1:n.130+1574G=
XR_926795.1:n.222+5906C=
XR_926796.1:n.214+5906C=
XR_926797.1:n.188+5906C=
XR_926795.2:n.517+5906C=
XR_926797.2:n.232+5906C=
NM_001271821.2:c.185G= NP_001258750.1:p.Arg62=
NM_018965.4:c.185G= MANE Select NP_061838.1:p.Arg62=