Canonical Allele Identifier: CA407854944

Gene: LILRB1

Linked Data

• gnomAD v4: 19-54636599-T-G
• MyVariant Identifiers: chr19:g.54636599T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54636599T>G , CM000681.2:g.54636599T>G	GRCh38
NC_000019.8:g.59839862T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324602.12:c.1759T>G MANE Select	ENSP00000315997.7:p.Phe587Val
ENST00000324602.11:c.1759T>G	ENSP00000315997.7:p.Phe587Val
ENST00000396315.5:c.1759T>G	ENSP00000379608.1:p.Phe587Val
ENST00000396317.5:c.1705T>G	ENSP00000379610.1:p.Phe569Val
ENST00000396327.7:c.1756T>G	ENSP00000379618.3:p.Phe586Val
ENST00000396331.5:c.1753T>G	ENSP00000379622.1:p.Phe585Val
ENST00000396332.8:c.1756T>G	ENSP00000379623.4:p.Phe586Val
ENST00000421584.5:c.1677T>G	ENSP00000410165.1:n.1677T>G
ENST00000427581.6:c.1906T>G	ENSP00000395004.2:p.Phe636Val
ENST00000462628.5:n.1537T>G
NM_001081637.2:c.1759T>G	NP_001075106.2:p.Phe587Val
NM_001081638.3:c.1756T>G	NP_001075107.2:p.Phe586Val
NM_001081639.3:c.1756T>G	NP_001075108.2:p.Phe586Val
NM_001278398.2:c.1705T>G	NP_001265327.2:p.Phe569Val
NM_006669.6:c.1753T>G	NP_006660.4:p.Phe585Val
NR_103518.2:n.1842T>G
XM_011526331.1:c.1789T>G	XP_011524633.1:p.Phe597Val
XM_011526332.1:c.1786T>G	XP_011524634.1:p.Phe596Val
XM_011526333.1:c.1786T>G	XP_011524635.1:p.Phe596Val
XM_011526334.1:c.1810T>G	XP_011524636.1:p.Phe604Val
XM_011526335.1:c.1684-133T>G	XP_011524637.1:n.1684-133T>G
XM_011526336.1:c.1651-133T>G	XP_011524638.1:n.1651-133T>G
XM_011526339.1:c.1753T>G	XP_011524641.1:p.Phe585Val
XM_011526331.2:c.1789T>G	XP_011524633.1:p.Phe597Val
XM_011526332.3:c.1786T>G	XP_011524634.1:p.Phe596Val
XM_011526335.2:c.1684-133T>G	XP_011524637.1:n.1684-133T>G
XM_011526336.2:c.1651-133T>G	XP_011524638.1:n.1651-133T>G
XM_017026182.2:c.1786T>G	XP_016881671.1:p.Phe596Val
XM_017026183.2:c.1783T>G	XP_016881672.1:p.Phe595Val
XM_017026184.2:c.1783T>G	XP_016881673.1:p.Phe595Val
XM_017026185.1:c.1753T>G	XP_016881674.1:p.Phe585Val
XM_017026186.1:c.1810T>G	XP_016881675.1:p.Phe604Val
XM_017026187.1:c.1810T>G	XP_016881676.1:p.Phe604Val
XM_017026188.1:c.1807T>G	XP_016881677.1:p.Phe603Val
XM_017026189.1:c.1807T>G	XP_016881678.1:p.Phe603Val
XM_017026190.1:c.1804T>G	XP_016881679.1:p.Phe602Val
XM_017026191.1:c.1654-133T>G	XP_016881680.1:n.1654-133T>G
XR_001753590.2:n.2006T>G
XR_001753591.1:n.2011T>G
XR_002958244.1:n.2003T>G
NM_001081637.3:c.1759T>G MANE Select	NP_001075106.2:p.Phe587Val
NM_001081638.4:c.1756T>G	NP_001075107.2:p.Phe586Val
NM_001081639.4:c.1756T>G	NP_001075108.2:p.Phe586Val
NM_001388355.1:c.1756T>G	NP_001375284.1:p.Phe586Val
NM_001388356.1:c.1756T>G	NP_001375285.1:p.Phe586Val
NM_001388357.1:c.1756T>G	NP_001375286.1:p.Phe586Val
NM_001388358.1:c.1759T>G	NP_001375287.1:p.Phe587Val
NM_006669.7:c.1753T>G	NP_006660.4:p.Phe585Val