Canonical Allele Identifier: CA138018666

Gene: TREM2

Linked Data

• dbSNP Id: rs750686409
• gnomAD v4: 6-41161352-T-G
• MyVariant Identifiers: chr6:g.41129090T>G (hg19) ; chr6:g.41161352T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161352T>G , CM000668.2:g.41161352T>G	GRCh38
NC_000006.11:g.41129090T>G , CM000668.1:g.41129090T>G	GRCh37
NC_000006.10:g.41237068T>G	NCBI36
NG_011561.1:g.6833A>C , LRG_631:g.6833A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373113.8:c.302A>C MANE Select	ENSP00000362205.3:p.Gln101Pro
ENST00000338469.3:c.302A>C	ENSP00000342651.4:p.Gln101Pro
ENST00000373113.7:c.302A>C	ENSP00000362205.3:p.Gln101Pro
ENST00000373122.8:c.302A>C	ENSP00000362214.4:p.Gln101Pro
NM_001271821.1:c.302A>C	NP_001258750.1:p.Gln101Pro
NM_018965.3:c.302A>C , LRG_631t1:c.302A>C	NP_061838.1:p.Gln101Pro
XM_006715116.2:c.131-1470A>C	XP_006715179.1:n.131-1470A>C
XR_926795.1:n.222+5789T>G
XR_926796.1:n.214+5789T>G
XR_926797.1:n.188+5789T>G
XR_926795.2:n.517+5789T>G
XR_926797.2:n.232+5789T>G
NM_001271821.2:c.302A>C	NP_001258750.1:p.Gln101Pro
NM_018965.4:c.302A>C MANE Select	NP_061838.1:p.Gln101Pro