Canonical Allele Identifier: CA1139922193
Gene: LBR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225419442C= , CM000663.2:g.225419442C= GRCh38
NC_000001.10:g.225607144C= , CM000663.1:g.225607144C= GRCh37
NC_000001.9:g.223673767C= NCBI36
NG_008099.1:g.14376G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272163.9:c.461G= MANE Select ENSP00000272163.4:p.Ser154=
ENST00000651341.1:c.461G= ENSP00000499114.1:p.Ser154=
ENST00000272163.8:c.461G= ENSP00000272163.4:p.Ser154=
ENST00000338179.6:c.461G= ENSP00000339883.2:p.Ser154=
ENST00000425080.1:c.461G= ENSP00000388059.1:p.Ser154=
NM_002296.3:c.461G= NP_002287.2:p.Ser154=
NM_194442.2:c.461G= NP_919424.1:p.Ser154=
XM_005273125.2:c.461G= XP_005273182.1:p.Ser154=
XM_011544185.1:c.461G= XP_011542487.1:p.Ser154=
XM_011544186.1:c.461G= XP_011542488.1:p.Ser154=
XM_011544187.1:c.461G= XP_011542489.1:p.Ser154=
XM_005273125.3:c.461G= XP_005273182.1:p.Ser154=
XM_011544185.3:c.461G= XP_011542487.1:p.Ser154=
XR_001737168.2:n.588G=
NM_002296.4:c.461G= MANE Select NP_002287.2:p.Ser154=
NM_194442.3:c.461G= NP_919424.1:p.Ser154=