Canonical Allele Identifier: CA138023308

Gene: TREM1

Linked Data

• dbSNP Id: rs887931690
• gnomAD v2: 6-41253976-T-C
• gnomAD v3: 6-41286238-T-C
• gnomAD v4: 6-41286238-T-C
• MyVariant Identifiers: chr6:g.41253976T>C (hg19) ; chr6:g.41286238T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41286238T>C , CM000668.2:g.41286238T>C	GRCh38
NC_000006.11:g.41253976T>C , CM000668.1:g.41253976T>C	GRCh37
NC_000006.10:g.41361954T>C	NCBI36
NG_029525.1:g.5482A>G
NG_029525.2:g.5482A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000244709.9:c.49+369A>G MANE Select	ENSP00000244709.3:n.49+369A>G
ENST00000244709.8:c.49+369A>G	ENSP00000244709.3:n.49+369A>G
ENST00000334475.10:c.49+369A>G	ENSP00000334284.5:n.49+369A>G
ENST00000586287.1:n.76+369A>G
ENST00000589614.5:c.49+369A>G	ENSP00000465688.1:n.49+369A>G
ENST00000591620.1:c.49+369A>G	ENSP00000465345.1:n.49+369A>G
NM_001242589.1:c.49+369A>G	NP_001229518.1:n.49+369A>G
NM_001242590.1:c.49+369A>G	NP_001229519.1:n.49+369A>G
NM_018643.3:c.49+369A>G	NP_061113.1:n.49+369A>G
XM_006715117.2:c.49+369A>G	XP_006715180.1:n.49+369A>G
XM_011514696.1:c.49+369A>G	XP_011512998.1:n.49+369A>G
XM_011514697.1:c.49+369A>G	XP_011512999.1:n.49+369A>G
NM_001242589.2:c.49+369A>G	NP_001229518.1:n.49+369A>G
NM_001242590.2:c.49+369A>G	NP_001229519.1:n.49+369A>G
NM_018643.4:c.49+369A>G	NP_061113.1:n.49+369A>G
NR_136332.1:n.139+369A>G
XM_006715117.3:c.49+369A>G	XP_006715180.1:n.49+369A>G
XM_011514696.2:c.49+369A>G	XP_011512998.1:n.49+369A>G
XM_017010956.2:c.49+369A>G	XP_016866445.1:n.49+369A>G
XM_017010957.1:c.49+369A>G	XP_016866446.1:n.49+369A>G
NM_018643.5:c.49+369A>G MANE Select	NP_061113.1:n.49+369A>G
NM_001242589.3:c.49+369A>G	NP_001229518.1:n.49+369A>G
NM_001242590.3:c.49+369A>G	NP_001229519.1:n.49+369A>G
NR_136332.2:n.76+369A>G