Canonical Allele Identifier: CA364059086

Gene: TREM2

Linked Data

• gnomAD v4: 6-41161476-A-G
• MyVariant Identifiers: chr6:g.41129214A>G (hg19) ; chr6:g.41161476A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161476A>G , CM000668.2:g.41161476A>G	GRCh38
NC_000006.11:g.41129214A>G , CM000668.1:g.41129214A>G	GRCh37
NC_000006.10:g.41237192A>G	NCBI36
NG_011561.1:g.6709T>C , LRG_631:g.6709T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373113.8:c.178T>C MANE Select	ENSP00000362205.3:p.Cys60Arg
ENST00000338469.3:c.178T>C	ENSP00000342651.4:p.Cys60Arg
ENST00000373113.7:c.178T>C	ENSP00000362205.3:p.Cys60Arg
ENST00000373122.8:c.178T>C	ENSP00000362214.4:p.Cys60Arg
NM_001271821.1:c.178T>C	NP_001258750.1:p.Cys60Arg
NM_018965.3:c.178T>C , LRG_631t1:c.178T>C	NP_061838.1:p.Cys60Arg
XM_006715116.2:c.130+1567T>C	XP_006715179.1:n.130+1567T>C
XR_926795.1:n.222+5913A>G
XR_926796.1:n.214+5913A>G
XR_926797.1:n.188+5913A>G
XR_926795.2:n.517+5913A>G
XR_926797.2:n.232+5913A>G
NM_001271821.2:c.178T>C	NP_001258750.1:p.Cys60Arg
NM_018965.4:c.178T>C MANE Select	NP_061838.1:p.Cys60Arg