Canonical Allele Identifier: CA364057592

Gene: TREM2

Linked Data

• MyVariant Identifiers: chr6:g.41126729C>G (hg19) ; chr6:g.41158991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41158991C>G , CM000668.2:g.41158991C>G	GRCh38
NC_000006.11:g.41126729C>G , CM000668.1:g.41126729C>G	GRCh37
NC_000006.10:g.41234707C>G	NCBI36
NG_011561.1:g.9194G>C , LRG_631:g.9194G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373113.8:c.558G>C MANE Select	ENSP00000362205.3:p.Lys186Asn
ENST00000338469.3:c.483-211G>C	ENSP00000342651.4:n.483-211G>C
ENST00000373113.7:c.558G>C	ENSP00000362205.3:p.Lys186Asn
ENST00000373122.8:c.598G>C	ENSP00000362214.4:p.Asp200His
NM_001271821.1:c.483-211G>C	NP_001258750.1:n.483-211G>C
NM_018965.3:c.558G>C , LRG_631t1:c.558G>C	NP_061838.1:p.Lys186Asn
XM_006715116.2:c.297G>C	XP_006715179.1:p.Lys99Asn
XR_926795.1:n.222+3428C>G
XR_926796.1:n.214+3428C>G
XR_926797.1:n.188+3428C>G
XR_926795.2:n.517+3428C>G
XR_926797.2:n.232+3428C>G
NM_001271821.2:c.483-211G>C	NP_001258750.1:n.483-211G>C
NM_018965.4:c.558G>C MANE Select	NP_061838.1:p.Lys186Asn