Canonical Allele Identifier: CA1623461367

Gene: TREM2

Linked Data

• dbSNP Id: rs1582079483

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161259T>C , CM000668.2:g.41161259T>C	GRCh38
NC_000006.11:g.41128997T>C , CM000668.1:g.41128997T>C	GRCh37
NC_000006.10:g.41236975T>C	NCBI36
NG_011561.1:g.6926A>G , LRG_631:g.6926A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.391+4A>G MANE Select	ENSP00000362205.3:n.391+4A>G
ENST00000338469.3:c.391+4A>G	ENSP00000342651.4:n.391+4A>G
ENST00000373113.7:c.391+4A>G	ENSP00000362205.3:n.391+4A>G
ENST00000373122.8:c.391+4A>G	ENSP00000362214.4:n.391+4A>G
NM_001271821.1:c.391+4A>G	NP_001258750.1:n.391+4A>G
NM_018965.3:c.391+4A>G , LRG_631t1:c.391+4A>G	NP_061838.1:n.391+4A>G
XM_006715116.2:c.131-1377A>G	XP_006715179.1:n.131-1377A>G
XR_926795.1:n.222+5696T>C
XR_926796.1:n.214+5696T>C
XR_926797.1:n.188+5696T>C
XR_926795.2:n.517+5696T>C
XR_926797.2:n.232+5696T>C
NM_001271821.2:c.391+4A>G	NP_001258750.1:n.391+4A>G
NM_018965.4:c.391+4A>G MANE Select	NP_061838.1:n.391+4A>G