Canonical Allele Identifier: CA2578613275
Gene: TREM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41161243G>T , CM000668.2:g.41161243G>T GRCh38
NC_000006.11:g.41128981G>T , CM000668.1:g.41128981G>T GRCh37
NC_000006.10:g.41236959G>T NCBI36
NG_011561.1:g.6942C>A , LRG_631:g.6942C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373113.8:c.391+20C>A MANE Select ENSP00000362205.3:n.391+20C>A
ENST00000338469.3:c.391+20C>A ENSP00000342651.4:n.391+20C>A
ENST00000373113.7:c.391+20C>A ENSP00000362205.3:n.391+20C>A
ENST00000373122.8:c.391+20C>A ENSP00000362214.4:n.391+20C>A
NM_001271821.1:c.391+20C>A NP_001258750.1:n.391+20C>A
NM_018965.3:c.391+20C>A , LRG_631t1:c.391+20C>A NP_061838.1:n.391+20C>A
XM_006715116.2:c.131-1361C>A XP_006715179.1:n.131-1361C>A
XR_926795.1:n.222+5680G>T
XR_926796.1:n.214+5680G>T
XR_926797.1:n.188+5680G>T
XR_926795.2:n.517+5680G>T
XR_926797.2:n.232+5680G>T
NM_001271821.2:c.391+20C>A NP_001258750.1:n.391+20C>A
NM_018965.4:c.391+20C>A MANE Select NP_061838.1:n.391+20C>A
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