Canonical Allele Identifier: CA38520247

Gene: LBR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225421980T>C , CM000663.2:g.225421980T>C	GRCh38
NC_000001.10:g.225609682T>C , CM000663.1:g.225609682T>C	GRCh37
NC_000001.9:g.223676305T>C	NCBI36
NG_008099.1:g.11838A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002296.4:c.366+97A>G MANE Select	NP_002287.2:n.366+97A>G
ENST00000272163.9:c.366+97A>G MANE Select	ENSP00000272163.4:n.366+97A>G
NM_002296.3:c.366+97A>G	NP_002287.2:n.366+97A>G
NM_194442.2:c.366+97A>G	NP_919424.1:n.366+97A>G
NM_194442.3:c.366+97A>G	NP_919424.1:n.366+97A>G
ENST00000272163.8:c.366+97A>G	ENSP00000272163.4:n.366+97A>G
ENST00000338179.6:c.366+97A>G	ENSP00000339883.2:n.366+97A>G
ENST00000425080.1:c.366+97A>G	ENSP00000388059.1:n.366+97A>G
ENST00000488632.1:n.351+97A>G
ENST00000651341.1:c.366+97A>G	ENSP00000499114.1:n.366+97A>G
XM_005273125.2:c.366+97A>G	XP_005273182.1:n.366+97A>G
XM_005273125.3:c.366+97A>G	XP_005273182.1:n.366+97A>G
XM_011544185.1:c.366+97A>G	XP_011542487.1:n.366+97A>G
XM_011544185.3:c.366+97A>G	XP_011542487.1:n.366+97A>G
XM_011544186.1:c.366+97A>G	XP_011542488.1:n.366+97A>G
XM_011544187.1:c.366+97A>G	XP_011542489.1:n.366+97A>G
XR_001737168.2:n.493+97A>G