Canonical Allele Identifier: CA364058808

Gene: TREM2

Linked Data

• gnomAD v4: 6-41161341-C-T
• MyVariant Identifiers: chr6:g.41129079C>T (hg19) ; chr6:g.41161341C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161341C>T , CM000668.2:g.41161341C>T	GRCh38
NC_000006.11:g.41129079C>T , CM000668.1:g.41129079C>T	GRCh37
NC_000006.10:g.41237057C>T	NCBI36
NG_011561.1:g.6844G>A , LRG_631:g.6844G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.313G>A MANE Select	ENSP00000362205.3:p.Ala105Thr
ENST00000338469.3:c.313G>A	ENSP00000342651.4:p.Ala105Thr
ENST00000373113.7:c.313G>A	ENSP00000362205.3:p.Ala105Thr
ENST00000373122.8:c.313G>A	ENSP00000362214.4:p.Ala105Thr
NM_001271821.1:c.313G>A	NP_001258750.1:p.Ala105Thr
NM_018965.3:c.313G>A , LRG_631t1:c.313G>A	NP_061838.1:p.Ala105Thr
XM_006715116.2:c.131-1459G>A	XP_006715179.1:n.131-1459G>A
XR_926795.1:n.222+5778C>T
XR_926796.1:n.214+5778C>T
XR_926797.1:n.188+5778C>T
XR_926795.2:n.517+5778C>T
XR_926797.2:n.232+5778C>T
NM_001271821.2:c.313G>A	NP_001258750.1:p.Ala105Thr
NM_018965.4:c.313G>A MANE Select	NP_061838.1:p.Ala105Thr