Canonical Allele Identifier: CA567147834

Gene: TREM2

Linked Data

• dbSNP Id: rs1268513553
• gnomAD v2: 6-41128993-C-A
• gnomAD v4: 6-41161255-C-A
• MyVariant Identifiers: chr6:g.41128993C>A (hg19) ; chr6:g.41161255C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161255C>A , CM000668.2:g.41161255C>A	GRCh38
NC_000006.11:g.41128993C>A , CM000668.1:g.41128993C>A	GRCh37
NC_000006.10:g.41236971C>A	NCBI36
NG_011561.1:g.6930G>T , LRG_631:g.6930G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.391+8G>T MANE Select	ENSP00000362205.3:n.391+8G>T
ENST00000338469.3:c.391+8G>T	ENSP00000342651.4:n.391+8G>T
ENST00000373113.7:c.391+8G>T	ENSP00000362205.3:n.391+8G>T
ENST00000373122.8:c.391+8G>T	ENSP00000362214.4:n.391+8G>T
NM_001271821.1:c.391+8G>T	NP_001258750.1:n.391+8G>T
NM_018965.3:c.391+8G>T , LRG_631t1:c.391+8G>T	NP_061838.1:n.391+8G>T
XM_006715116.2:c.131-1373G>T	XP_006715179.1:n.131-1373G>T
XR_926795.1:n.222+5692C>A
XR_926796.1:n.214+5692C>A
XR_926797.1:n.188+5692C>A
XR_926795.2:n.517+5692C>A
XR_926797.2:n.232+5692C>A
NM_001271821.2:c.391+8G>T	NP_001258750.1:n.391+8G>T
NM_018965.4:c.391+8G>T MANE Select	NP_061838.1:n.391+8G>T