Canonical Allele Identifier: CA364059260

Gene: TREM2

Linked Data

• MyVariant Identifiers: chr6:g.41129295G>C (hg19) ; chr6:g.41161557G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161557G>C , CM000668.2:g.41161557G>C	GRCh38
NC_000006.11:g.41129295G>C , CM000668.1:g.41129295G>C	GRCh37
NC_000006.10:g.41237273G>C	NCBI36
NG_011561.1:g.6628C>G , LRG_631:g.6628C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.97C>G MANE Select	ENSP00000362205.3:p.Gln33Glu
ENST00000338469.3:c.97C>G	ENSP00000342651.4:p.Gln33Glu
ENST00000373113.7:c.97C>G	ENSP00000362205.3:p.Gln33Glu
ENST00000373122.8:c.97C>G	ENSP00000362214.4:p.Gln33Glu
NM_001271821.1:c.97C>G	NP_001258750.1:p.Gln33Glu
NM_018965.3:c.97C>G , LRG_631t1:c.97C>G	NP_061838.1:p.Gln33Glu
XM_006715116.2:c.130+1486C>G	XP_006715179.1:n.130+1486C>G
XR_926795.1:n.222+5994G>C
XR_926796.1:n.214+5994G>C
XR_926797.1:n.188+5994G>C
XR_926795.2:n.517+5994G>C
XR_926797.2:n.232+5994G>C
NM_001271821.2:c.97C>G	NP_001258750.1:p.Gln33Glu
NM_018965.4:c.97C>G MANE Select	NP_061838.1:p.Gln33Glu