Canonical Allele Identifier: CA407854985

Gene: LILRB1

Linked Data

• MyVariant Identifiers: chr19:g.54636612A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54636612A>T , CM000681.2:g.54636612A>T	GRCh38
NC_000019.8:g.59839875A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324602.12:c.1772A>T MANE Select	ENSP00000315997.7:p.Lys591Met
ENST00000324602.11:c.1772A>T	ENSP00000315997.7:p.Lys591Met
ENST00000396315.5:c.1772A>T	ENSP00000379608.1:p.Lys591Met
ENST00000396317.5:c.1718A>T	ENSP00000379610.1:p.Lys573Met
ENST00000396327.7:c.1769A>T	ENSP00000379618.3:p.Lys590Met
ENST00000396331.5:c.1766A>T	ENSP00000379622.1:p.Lys589Met
ENST00000396332.8:c.1769A>T	ENSP00000379623.4:p.Lys590Met
ENST00000421584.5:c.1690A>T	ENSP00000410165.1:n.1690A>T
ENST00000427581.6:c.1919A>T	ENSP00000395004.2:p.Lys640Met
ENST00000462628.5:n.1550A>T
NM_001081637.2:c.1772A>T	NP_001075106.2:p.Lys591Met
NM_001081638.3:c.1769A>T	NP_001075107.2:p.Lys590Met
NM_001081639.3:c.1769A>T	NP_001075108.2:p.Lys590Met
NM_001278398.2:c.1718A>T	NP_001265327.2:p.Lys573Met
NM_006669.6:c.1766A>T	NP_006660.4:p.Lys589Met
NR_103518.2:n.1855A>T
XM_011526331.1:c.1802A>T	XP_011524633.1:p.Lys601Met
XM_011526332.1:c.1799A>T	XP_011524634.1:p.Lys600Met
XM_011526333.1:c.1799A>T	XP_011524635.1:p.Lys600Met
XM_011526334.1:c.1823A>T	XP_011524636.1:p.Lys608Met
XM_011526335.1:c.1684-120A>T	XP_011524637.1:n.1684-120A>T
XM_011526336.1:c.1651-120A>T	XP_011524638.1:n.1651-120A>T
XM_011526339.1:c.1766A>T	XP_011524641.1:p.Lys589Met
XM_011526331.2:c.1802A>T	XP_011524633.1:p.Lys601Met
XM_011526332.3:c.1799A>T	XP_011524634.1:p.Lys600Met
XM_011526335.2:c.1684-120A>T	XP_011524637.1:n.1684-120A>T
XM_011526336.2:c.1651-120A>T	XP_011524638.1:n.1651-120A>T
XM_017026182.2:c.1799A>T	XP_016881671.1:p.Lys600Met
XM_017026183.2:c.1796A>T	XP_016881672.1:p.Lys599Met
XM_017026184.2:c.1796A>T	XP_016881673.1:p.Lys599Met
XM_017026185.1:c.1766A>T	XP_016881674.1:p.Lys589Met
XM_017026186.1:c.1823A>T	XP_016881675.1:p.Lys608Met
XM_017026187.1:c.1823A>T	XP_016881676.1:p.Lys608Met
XM_017026188.1:c.1820A>T	XP_016881677.1:p.Lys607Met
XM_017026189.1:c.1820A>T	XP_016881678.1:p.Lys607Met
XM_017026190.1:c.1817A>T	XP_016881679.1:p.Lys606Met
XM_017026191.1:c.1654-120A>T	XP_016881680.1:n.1654-120A>T
XR_001753590.2:n.2019A>T
XR_001753591.1:n.2024A>T
XR_002958244.1:n.2016A>T
NM_001081637.3:c.1772A>T MANE Select	NP_001075106.2:p.Lys591Met
NM_001081638.4:c.1769A>T	NP_001075107.2:p.Lys590Met
NM_001081639.4:c.1769A>T	NP_001075108.2:p.Lys590Met
NM_001388355.1:c.1769A>T	NP_001375284.1:p.Lys590Met
NM_001388356.1:c.1769A>T	NP_001375285.1:p.Lys590Met
NM_001388357.1:c.1769A>T	NP_001375286.1:p.Lys590Met
NM_001388358.1:c.1772A>T	NP_001375287.1:p.Lys591Met
NM_006669.7:c.1766A>T	NP_006660.4:p.Lys589Met