Canonical Allele Identifier: CA2342975288
Community Standard Title: NM_001081637.3(LILRB1):c.1879G= (p.Glu627=)
Gene: LILRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54636798G= , CM000681.2:g.54636798G= GRCh38
NC_000019.8:g.59840061G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001081637.3:c.1879G= MANE Select NP_001075106.2:p.Glu627=
ENST00000324602.12:c.1879G= MANE Select ENSP00000315997.7:p.Glu627=
NM_001081637.2:c.1879G= NP_001075106.2:p.Glu627=
NM_001081638.3:c.1876G= NP_001075107.2:p.Glu626=
NM_001081638.4:c.1876G= NP_001075107.2:p.Glu626=
NM_001081639.3:c.1876G= NP_001075108.2:p.Glu626=
NM_001081639.4:c.1876G= NP_001075108.2:p.Glu626=
NM_001278398.2:c.1825G= NP_001265327.2:p.Glu609=
NM_001388355.1:c.1876G= NP_001375284.1:p.Glu626=
NM_001388356.1:c.1876G= NP_001375285.1:p.Glu626=
NM_001388357.1:c.1876G= NP_001375286.1:p.Glu626=
NM_001388358.1:c.1879G= NP_001375287.1:p.Glu627=
NM_006669.6:c.1873G= NP_006660.4:p.Glu625=
NM_006669.7:c.1873G= NP_006660.4:p.Glu625=
NR_103518.2:n.1962G=
ENST00000324602.11:c.1879G= ENSP00000315997.7:p.Glu627=
ENST00000396315.5:c.1879G= ENSP00000379608.1:p.Glu627=
ENST00000396317.5:c.1825G= ENSP00000379610.1:p.Glu609=
ENST00000396327.7:c.1876G= ENSP00000379618.3:p.Glu626=
ENST00000396331.5:c.1873G= ENSP00000379622.1:p.Glu625=
ENST00000396332.8:c.1876G= ENSP00000379623.4:p.Glu626=
ENST00000421584.5:c.1797G= ENSP00000410165.1:n.1797G=
ENST00000427581.6:c.2026G= ENSP00000395004.2:p.Glu676=
ENST00000462628.5:n.1657G=
XM_011526331.1:c.1909G= XP_011524633.1:p.Glu637=
XM_011526331.2:c.1909G= XP_011524633.1:p.Glu637=
XM_011526332.1:c.1906G= XP_011524634.1:p.Glu636=
XM_011526332.3:c.1906G= XP_011524634.1:p.Glu636=
XM_011526333.1:c.1906G= XP_011524635.1:p.Glu636=
XM_011526334.1:c.1930G= XP_011524636.1:p.Glu644=
XM_011526335.1:c.1750G= XP_011524637.1:p.Glu584=
XM_011526335.2:c.1750G= XP_011524637.1:p.Glu584=
XM_011526336.1:c.1717G= XP_011524638.1:p.Glu573=
XM_011526336.2:c.1717G= XP_011524638.1:p.Glu573=
XM_011526339.1:c.1873G= XP_011524641.1:p.Glu625=
XM_017026182.2:c.1906G= XP_016881671.1:p.Glu636=
XM_017026183.2:c.1903G= XP_016881672.1:p.Glu635=
XM_017026184.2:c.1903G= XP_016881673.1:p.Glu635=
XM_017026185.1:c.1873G= XP_016881674.1:p.Glu625=
XM_017026186.1:c.1930G= XP_016881675.1:p.Glu644=
XM_017026187.1:c.1930G= XP_016881676.1:p.Glu644=
XM_017026188.1:c.1927G= XP_016881677.1:p.Glu643=
XM_017026189.1:c.1927G= XP_016881678.1:p.Glu643=
XM_017026190.1:c.1924G= XP_016881679.1:p.Glu642=
XM_017026191.1:c.1720G= XP_016881680.1:p.Glu574=
XR_001753590.2:n.2126G=
XR_001753591.1:n.2131G=
XR_002958244.1:n.2123G=