Canonical Allele Identifier: CA450354182

Gene: TREM2

Linked Data

• MyVariant Identifiers: chr6:g.41129002T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161264T>G , CM000668.2:g.41161264T>G	GRCh38
NC_000006.11:g.41129002T>G , CM000668.1:g.41129002T>G	GRCh37
NC_000006.10:g.41236980T>G	NCBI36
NG_011561.1:g.6921A>C , LRG_631:g.6921A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.390A>C MANE Select	ENSP00000362205.3:p.Ala130=
ENST00000338469.3:c.390A>C	ENSP00000342651.4:p.Ala130=
ENST00000373113.7:c.390A>C	ENSP00000362205.3:p.Ala130=
ENST00000373122.8:c.390A>C	ENSP00000362214.4:p.Ala130=
NM_001271821.1:c.390A>C	NP_001258750.1:p.Ala130=
NM_018965.3:c.390A>C , LRG_631t1:c.390A>C	NP_061838.1:p.Ala130=
XM_006715116.2:c.131-1382A>C	XP_006715179.1:n.131-1382A>C
XR_926795.1:n.222+5701T>G
XR_926796.1:n.214+5701T>G
XR_926797.1:n.188+5701T>G
XR_926795.2:n.517+5701T>G
XR_926797.2:n.232+5701T>G
NM_001271821.2:c.390A>C	NP_001258750.1:p.Ala130=
NM_018965.4:c.390A>C MANE Select	NP_061838.1:p.Ala130=