Canonical Allele Identifier: CA138023117

Gene: TREM1

Linked Data

• dbSNP Id: rs6921317
• gnomAD v2: 6-41253775-A-G
• gnomAD v3: 6-41286037-A-G
• gnomAD v4: 6-41286037-A-G
• MyVariant Identifiers: chr6:g.41253775A>G (hg19) ; chr6:g.41286037A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41286037A>G , CM000668.2:g.41286037A>G	GRCh38
NC_000006.11:g.41253775A>G , CM000668.1:g.41253775A>G	GRCh37
NC_000006.10:g.41361753A>G	NCBI36
NG_029525.1:g.5683T>C
NG_029525.2:g.5683T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244709.9:c.49+570T>C MANE Select	ENSP00000244709.3:n.49+570T>C
ENST00000244709.8:c.49+570T>C	ENSP00000244709.3:n.49+570T>C
ENST00000334475.10:c.49+570T>C	ENSP00000334284.5:n.49+570T>C
ENST00000586287.1:n.76+570T>C
ENST00000589614.5:c.49+570T>C	ENSP00000465688.1:n.49+570T>C
ENST00000591620.1:c.49+570T>C	ENSP00000465345.1:n.49+570T>C
NM_001242589.1:c.49+570T>C	NP_001229518.1:n.49+570T>C
NM_001242590.1:c.49+570T>C	NP_001229519.1:n.49+570T>C
NM_018643.3:c.49+570T>C	NP_061113.1:n.49+570T>C
XM_006715117.2:c.49+570T>C	XP_006715180.1:n.49+570T>C
XM_011514696.1:c.49+570T>C	XP_011512998.1:n.49+570T>C
XM_011514697.1:c.49+570T>C	XP_011512999.1:n.49+570T>C
NM_001242589.2:c.49+570T>C	NP_001229518.1:n.49+570T>C
NM_001242590.2:c.49+570T>C	NP_001229519.1:n.49+570T>C
NM_018643.4:c.49+570T>C	NP_061113.1:n.49+570T>C
NR_136332.1:n.139+570T>C
XM_006715117.3:c.49+570T>C	XP_006715180.1:n.49+570T>C
XM_011514696.2:c.49+570T>C	XP_011512998.1:n.49+570T>C
XM_017010956.2:c.49+570T>C	XP_016866445.1:n.49+570T>C
XM_017010957.1:c.49+570T>C	XP_016866446.1:n.49+570T>C
NM_018643.5:c.49+570T>C MANE Select	NP_061113.1:n.49+570T>C
NM_001242589.3:c.49+570T>C	NP_001229518.1:n.49+570T>C
NM_001242590.3:c.49+570T>C	NP_001229519.1:n.49+570T>C
NR_136332.2:n.76+570T>C