Canonical Allele Identifier: CA360721851
Gene: LMNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126810315T>C , CM000667.2:g.126810315T>C GRCh38
NC_000005.9:g.126146007T>C , CM000667.1:g.126146007T>C GRCh37
NC_000005.8:g.126173906T>C NCBI36
NG_008360.2:g.38175T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261366.10:c.778T>C MANE Select ENSP00000261366.5:p.Tyr260His
ENST00000261366.9:c.778T>C ENSP00000261366.5:p.Tyr260His
ENST00000395354.1:c.778T>C ENSP00000378761.1:p.Tyr260His
ENST00000460265.5:c.778T>C ENSP00000486528.1:p.Tyr260His
ENST00000472034.5:n.511T>C
ENST00000504788.5:n.511T>C
NM_001198557.1:c.148T>C NP_001185486.1:p.Tyr50His
NM_005573.3:c.778T>C NP_005564.1:p.Tyr260His
XR_948250.1:n.1142T>C
NR_134488.1:n.1664T>C
NM_005573.4:c.778T>C MANE Select NP_005564.1:p.Tyr260His
NM_001198557.2:c.148T>C NP_001185486.1:p.Tyr50His