Canonical Allele Identifier: CA1417574

Gene: LBR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225423986G>A , CM000663.2:g.225423986G>A	GRCh38
NC_000001.10:g.225611688G>A , CM000663.1:g.225611688G>A	GRCh37
NC_000001.9:g.223678311G>A	NCBI36
NG_008099.1:g.9832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272163.9:c.90C>T MANE Select	ENSP00000272163.4:p.His30=
ENST00000651341.1:c.90C>T	ENSP00000499114.1:p.His30=
ENST00000272163.8:c.90C>T	ENSP00000272163.4:p.His30=
ENST00000338179.6:c.90C>T	ENSP00000339883.2:p.His30=
ENST00000421383.1:c.90C>T	ENSP00000416554.1:p.His30=
ENST00000425080.1:c.90C>T	ENSP00000388059.1:p.His30=
NM_002296.3:c.90C>T	NP_002287.2:p.His30=
NM_194442.2:c.90C>T	NP_919424.1:p.His30=
XM_005273125.2:c.90C>T	XP_005273182.1:p.His30=
XM_011544185.1:c.90C>T	XP_011542487.1:p.His30=
XM_011544186.1:c.90C>T	XP_011542488.1:p.His30=
XM_011544187.1:c.90C>T	XP_011542489.1:p.His30=
XM_005273125.3:c.90C>T	XP_005273182.1:p.His30=
XM_011544185.3:c.90C>T	XP_011542487.1:p.His30=
XR_001737168.2:n.217C>T
NM_002296.4:c.90C>T MANE Select	NP_002287.2:p.His30=
NM_194442.3:c.90C>T	NP_919424.1:p.His30=