Canonical Allele Identifier: CA1623461471
Gene: TREM2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000373113.8:c.302A= MANE Select ENSP00000362205.3:p.Gln101=
ENST00000338469.3:c.302A= ENSP00000342651.4:p.Gln101=
ENST00000373113.7:c.302A= ENSP00000362205.3:p.Gln101=
ENST00000373122.8:c.302A= ENSP00000362214.4:p.Gln101=
NM_001271821.1:c.302A= NP_001258750.1:p.Gln101=
NM_018965.3:c.302A= , LRG_631t1:c.302A= NP_061838.1:p.Gln101=
XM_006715116.2:c.131-1470A= XP_006715179.1:n.131-1470A=
XR_926795.1:n.222+5789T=
XR_926796.1:n.214+5789T=
XR_926797.1:n.188+5789T=
XR_926795.2:n.517+5789T=
XR_926797.2:n.232+5789T=
NM_001271821.2:c.302A= NP_001258750.1:p.Gln101=
NM_018965.4:c.302A= MANE Select NP_061838.1:p.Gln101=