Canonical Allele Identifier: CA883649062

Gene: LILRB1

Linked Data

• dbSNP Id: rs574818482
• gnomAD v3: 19-54636691-C-G
• gnomAD v4: 19-54636691-C-G
• MyVariant Identifiers: chr19:g.54636691C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54636691C>G , CM000681.2:g.54636691C>G	GRCh38
NC_000019.8:g.59839954C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324602.12:c.1812+39C>G MANE Select	ENSP00000315997.7:n.1812+39C>G
ENST00000324602.11:c.1812+39C>G	ENSP00000315997.7:n.1812+39C>G
ENST00000396315.5:c.1812+39C>G	ENSP00000379608.1:n.1812+39C>G
ENST00000396317.5:c.1758+39C>G	ENSP00000379610.1:n.1758+39C>G
ENST00000396327.7:c.1809+39C>G	ENSP00000379618.3:n.1809+39C>G
ENST00000396331.5:c.1806+39C>G	ENSP00000379622.1:n.1806+39C>G
ENST00000396332.8:c.1809+39C>G	ENSP00000379623.4:n.1809+39C>G
ENST00000421584.5:c.1730+39C>G	ENSP00000410165.1:n.1730+39C>G
ENST00000427581.6:c.1959+39C>G	ENSP00000395004.2:n.1959+39C>G
ENST00000462628.5:n.1590+39C>G
NM_001081637.2:c.1812+39C>G	NP_001075106.2:n.1812+39C>G
NM_001081638.3:c.1809+39C>G	NP_001075107.2:n.1809+39C>G
NM_001081639.3:c.1809+39C>G	NP_001075108.2:n.1809+39C>G
NM_001278398.2:c.1758+39C>G	NP_001265327.2:n.1758+39C>G
NM_006669.6:c.1806+39C>G	NP_006660.4:n.1806+39C>G
NR_103518.2:n.1895+39C>G
XM_011526331.1:c.1842+39C>G	XP_011524633.1:n.1842+39C>G
XM_011526332.1:c.1839+39C>G	XP_011524634.1:n.1839+39C>G
XM_011526333.1:c.1839+39C>G	XP_011524635.1:n.1839+39C>G
XM_011526334.1:c.1863+39C>G	XP_011524636.1:n.1863+39C>G
XM_011526335.1:c.1684-41C>G	XP_011524637.1:n.1684-41C>G
XM_011526336.1:c.1651-41C>G	XP_011524638.1:n.1651-41C>G
XM_011526339.1:c.1806+39C>G	XP_011524641.1:n.1806+39C>G
XM_011526331.2:c.1842+39C>G	XP_011524633.1:n.1842+39C>G
XM_011526332.3:c.1839+39C>G	XP_011524634.1:n.1839+39C>G
XM_011526335.2:c.1684-41C>G	XP_011524637.1:n.1684-41C>G
XM_011526336.2:c.1651-41C>G	XP_011524638.1:n.1651-41C>G
XM_017026182.2:c.1839+39C>G	XP_016881671.1:n.1839+39C>G
XM_017026183.2:c.1836+39C>G	XP_016881672.1:n.1836+39C>G
XM_017026184.2:c.1836+39C>G	XP_016881673.1:n.1836+39C>G
XM_017026185.1:c.1806+39C>G	XP_016881674.1:n.1806+39C>G
XM_017026186.1:c.1863+39C>G	XP_016881675.1:n.1863+39C>G
XM_017026187.1:c.1863+39C>G	XP_016881676.1:n.1863+39C>G
XM_017026188.1:c.1860+39C>G	XP_016881677.1:n.1860+39C>G
XM_017026189.1:c.1860+39C>G	XP_016881678.1:n.1860+39C>G
XM_017026190.1:c.1857+39C>G	XP_016881679.1:n.1857+39C>G
XM_017026191.1:c.1654-41C>G	XP_016881680.1:n.1654-41C>G
XR_001753590.2:n.2059+39C>G
XR_001753591.1:n.2064+39C>G
XR_002958244.1:n.2056+39C>G
NM_001081637.3:c.1812+39C>G MANE Select	NP_001075106.2:n.1812+39C>G
NM_001081638.4:c.1809+39C>G	NP_001075107.2:n.1809+39C>G
NM_001081639.4:c.1809+39C>G	NP_001075108.2:n.1809+39C>G
NM_001388355.1:c.1809+39C>G	NP_001375284.1:n.1809+39C>G
NM_001388356.1:c.1809+39C>G	NP_001375285.1:n.1809+39C>G
NM_001388357.1:c.1809+39C>G	NP_001375286.1:n.1809+39C>G
NM_001388358.1:c.1812+39C>G	NP_001375287.1:n.1812+39C>G
NM_006669.7:c.1806+39C>G	NP_006660.4:n.1806+39C>G