Canonical Allele Identifier: CA138019063

Gene: TREM2

Linked Data

• dbSNP Id: rs1047512297
• MyVariant Identifiers: chr6:g.41129311C>A (hg19) ; chr6:g.41161573C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161573C>A , CM000668.2:g.41161573C>A	GRCh38
NC_000006.11:g.41129311C>A , CM000668.1:g.41129311C>A	GRCh37
NC_000006.10:g.41237289C>A	NCBI36
NG_011561.1:g.6612G>T , LRG_631:g.6612G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.81G>T MANE Select	ENSP00000362205.3:p.Val27=
ENST00000338469.3:c.81G>T	ENSP00000342651.4:p.Val27=
ENST00000373113.7:c.81G>T	ENSP00000362205.3:p.Val27=
ENST00000373122.8:c.81G>T	ENSP00000362214.4:p.Val27=
NM_001271821.1:c.81G>T	NP_001258750.1:p.Val27=
NM_018965.3:c.81G>T , LRG_631t1:c.81G>T	NP_061838.1:p.Val27=
XM_006715116.2:c.130+1470G>T	XP_006715179.1:n.130+1470G>T
XR_926795.1:n.222+6010C>A
XR_926796.1:n.214+6010C>A
XR_926797.1:n.188+6010C>A
XR_926795.2:n.517+6010C>A
XR_926797.2:n.232+6010C>A
NM_001271821.2:c.81G>T	NP_001258750.1:p.Val27=
NM_018965.4:c.81G>T MANE Select	NP_061838.1:p.Val27=