Canonical Allele Identifier: CA360723980
Gene: LMNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126777509A>G , CM000667.2:g.126777509A>G GRCh38
NC_000005.9:g.126113201A>G , CM000667.1:g.126113201A>G GRCh37
NC_000005.8:g.126141100A>G NCBI36
NG_008360.2:g.5369A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261366.10:c.1A>G MANE Select ENSP00000261366.5:p.Met1Val
ENST00000261366.9:c.1A>G ENSP00000261366.5:p.Met1Val
ENST00000395354.1:c.1A>G ENSP00000378761.1:p.Met1Val
ENST00000460265.5:c.1A>G ENSP00000486528.1:p.Met1Val
ENST00000463908.2:n.28+103A>G
ENST00000472034.5:n.92+257A>G
ENST00000492190.5:c.1A>G ENSP00000486992.1:p.Met1Val
ENST00000504788.5:n.92+265A>G
NM_001198557.1:c.-272+265A>G NP_001185486.1:n.-272+265A>G
NM_005573.3:c.1A>G NP_005564.1:p.Met1Val
XR_948250.1:n.365A>G
NR_134488.1:n.887A>G
NM_005573.4:c.1A>G MANE Select NP_005564.1:p.Met1Val
NM_001198557.2:c.-272+265A>G NP_001185486.1:n.-272+265A>G