Canonical Allele Identifier: CA10622464

Gene: LMNB1

Linked Data

• ClinVar Variation Id: 350610
• ClinVar RCV Id: RCV000373329
• dbSNP Id: rs886059857
• MyVariant Identifiers: chr5:g.126113042C>G (hg19) ; chr5:g.126777350C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.126777350C>G , CM000667.2:g.126777350C>G	GRCh38
NC_000005.9:g.126113042C>G , CM000667.1:g.126113042C>G	GRCh37
NC_000005.8:g.126140941C>G	NCBI36
NG_008360.2:g.5210C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261366.10:c.-159C>G MANE Select	ENSP00000261366.5:n.-159C>G
ENST00000261366.9:c.-159C>G	ENSP00000261366.5:n.-159C>G
ENST00000395354.1:c.-159C>G	ENSP00000378761.1:n.-159C>G
ENST00000460265.5:c.-159C>G	ENSP00000486528.1:n.-159C>G
ENST00000472034.5:n.92+98C>G
ENST00000492190.5:c.-148-11C>G	ENSP00000486992.1:n.-148-11C>G
ENST00000504788.5:n.92+106C>G
NM_001198557.1:c.-272+106C>G	NP_001185486.1:n.-272+106C>G
NM_005573.3:c.-159C>G	NP_005564.1:n.-159C>G
XR_948250.1:n.206C>G
NR_134488.1:n.728C>G
NM_005573.4:c.-159C>G MANE Select	NP_005564.1:n.-159C>G
NM_001198557.2:c.-272+106C>G	NP_001185486.1:n.-272+106C>G