Canonical Allele Identifier: CA3798873

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41159785G>A , CM000668.2:g.41159785G>A	GRCh38
NC_000006.11:g.41127523G>A , CM000668.1:g.41127523G>A	GRCh37
NC_000006.10:g.41235501G>A	NCBI36
NG_011561.1:g.8400C>T , LRG_631:g.8400C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018965.4:c.482+7C>T MANE Select	NP_061838.1:n.482+7C>T
ENST00000373113.8:c.482+7C>T MANE Select	ENSP00000362205.3:n.482+7C>T
NM_001271821.1:c.482+7C>T	NP_001258750.1:n.482+7C>T
NM_001271821.2:c.482+7C>T	NP_001258750.1:n.482+7C>T
NM_018965.3:c.482+7C>T , LRG_631t1:c.482+7C>T	NP_061838.1:n.482+7C>T
ENST00000338469.3:c.482+7C>T	ENSP00000342651.4:n.482+7C>T
ENST00000373113.7:c.482+7C>T	ENSP00000362205.3:n.482+7C>T
ENST00000373122.8:c.482+7C>T	ENSP00000362214.4:n.482+7C>T
XM_006715116.2:c.221+7C>T	XP_006715179.1:n.221+7C>T
XR_926795.1:n.222+4222G>A
XR_926795.2:n.517+4222G>A
XR_926796.1:n.214+4222G>A
XR_926797.1:n.188+4222G>A
XR_926797.2:n.232+4222G>A