Canonical Allele Identifier: CA407854979

Gene: LILRB1

Linked Data

• dbSNP Id: rs1599874152
• MyVariant Identifiers: chr19:g.54636609C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54636609C>T , CM000681.2:g.54636609C>T	GRCh38
NC_000019.8:g.59839872C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324602.12:c.1769C>T MANE Select	ENSP00000315997.7:p.Thr590Ile
ENST00000324602.11:c.1769C>T	ENSP00000315997.7:p.Thr590Ile
ENST00000396315.5:c.1769C>T	ENSP00000379608.1:p.Thr590Ile
ENST00000396317.5:c.1715C>T	ENSP00000379610.1:p.Thr572Ile
ENST00000396327.7:c.1766C>T	ENSP00000379618.3:p.Thr589Ile
ENST00000396331.5:c.1763C>T	ENSP00000379622.1:p.Thr588Ile
ENST00000396332.8:c.1766C>T	ENSP00000379623.4:p.Thr589Ile
ENST00000421584.5:c.1687C>T	ENSP00000410165.1:n.1687C>T
ENST00000427581.6:c.1916C>T	ENSP00000395004.2:p.Thr639Ile
ENST00000462628.5:n.1547C>T
NM_001081637.2:c.1769C>T	NP_001075106.2:p.Thr590Ile
NM_001081638.3:c.1766C>T	NP_001075107.2:p.Thr589Ile
NM_001081639.3:c.1766C>T	NP_001075108.2:p.Thr589Ile
NM_001278398.2:c.1715C>T	NP_001265327.2:p.Thr572Ile
NM_006669.6:c.1763C>T	NP_006660.4:p.Thr588Ile
NR_103518.2:n.1852C>T
XM_011526331.1:c.1799C>T	XP_011524633.1:p.Thr600Ile
XM_011526332.1:c.1796C>T	XP_011524634.1:p.Thr599Ile
XM_011526333.1:c.1796C>T	XP_011524635.1:p.Thr599Ile
XM_011526334.1:c.1820C>T	XP_011524636.1:p.Thr607Ile
XM_011526335.1:c.1684-123C>T	XP_011524637.1:n.1684-123C>T
XM_011526336.1:c.1651-123C>T	XP_011524638.1:n.1651-123C>T
XM_011526339.1:c.1763C>T	XP_011524641.1:p.Thr588Ile
XM_011526331.2:c.1799C>T	XP_011524633.1:p.Thr600Ile
XM_011526332.3:c.1796C>T	XP_011524634.1:p.Thr599Ile
XM_011526335.2:c.1684-123C>T	XP_011524637.1:n.1684-123C>T
XM_011526336.2:c.1651-123C>T	XP_011524638.1:n.1651-123C>T
XM_017026182.2:c.1796C>T	XP_016881671.1:p.Thr599Ile
XM_017026183.2:c.1793C>T	XP_016881672.1:p.Thr598Ile
XM_017026184.2:c.1793C>T	XP_016881673.1:p.Thr598Ile
XM_017026185.1:c.1763C>T	XP_016881674.1:p.Thr588Ile
XM_017026186.1:c.1820C>T	XP_016881675.1:p.Thr607Ile
XM_017026187.1:c.1820C>T	XP_016881676.1:p.Thr607Ile
XM_017026188.1:c.1817C>T	XP_016881677.1:p.Thr606Ile
XM_017026189.1:c.1817C>T	XP_016881678.1:p.Thr606Ile
XM_017026190.1:c.1814C>T	XP_016881679.1:p.Thr605Ile
XM_017026191.1:c.1654-123C>T	XP_016881680.1:n.1654-123C>T
XR_001753590.2:n.2016C>T
XR_001753591.1:n.2021C>T
XR_002958244.1:n.2013C>T
NM_001081637.3:c.1769C>T MANE Select	NP_001075106.2:p.Thr590Ile
NM_001081638.4:c.1766C>T	NP_001075107.2:p.Thr589Ile
NM_001081639.4:c.1766C>T	NP_001075108.2:p.Thr589Ile
NM_001388355.1:c.1766C>T	NP_001375284.1:p.Thr589Ile
NM_001388356.1:c.1766C>T	NP_001375285.1:p.Thr589Ile
NM_001388357.1:c.1766C>T	NP_001375286.1:p.Thr589Ile
NM_001388358.1:c.1769C>T	NP_001375287.1:p.Thr590Ile
NM_006669.7:c.1763C>T	NP_006660.4:p.Thr588Ile