Canonical Allele Identifier: CA360722896

Gene: LMNB1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126811772G>T , CM000667.2:g.126811772G>T	GRCh38
NC_000005.9:g.126147464G>T , CM000667.1:g.126147464G>T	GRCh37
NC_000005.8:g.126175363G>T	NCBI36
NG_008360.2:g.39632G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261366.10:c.814-1G>T MANE Select	ENSP00000261366.5:n.814-1G>T
ENST00000261366.9:c.814-1G>T	ENSP00000261366.5:n.814-1G>T
ENST00000395354.1:c.814-1G>T	ENSP00000378761.1:n.814-1G>T
ENST00000460265.5:c.814-1G>T	ENSP00000486528.1:n.814-1G>T
ENST00000472034.5:n.547-1G>T
ENST00000494185.1:n.60G>T
ENST00000504788.5:n.547-1G>T
NM_001198557.1:c.184-1G>T	NP_001185486.1:n.184-1G>T
NM_005573.3:c.814-1G>T	NP_005564.1:n.814-1G>T
XR_948250.1:n.1178-1G>T
NR_134488.1:n.1700-1G>T
NM_005573.4:c.814-1G>T MANE Select	NP_005564.1:n.814-1G>T
NM_001198557.2:c.184-1G>T	NP_001185486.1:n.184-1G>T