Canonical Allele Identifier: CA10575509

Gene: LBR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225404715T>C , CM000663.2:g.225404715T>C	GRCh38
NC_000001.10:g.225592417T>C , CM000663.1:g.225592417T>C	GRCh37
NC_000001.9:g.223659040T>C	NCBI36
NG_008099.1:g.29103A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272163.9:c.1484-9A>G MANE Select	ENSP00000272163.4:n.1484-9A>G
ENST00000651341.1:c.*650-9A>G	ENSP00000499114.1:n.*650-9A>G
ENST00000272163.8:c.1484-9A>G	ENSP00000272163.4:n.1484-9A>G
ENST00000338179.6:c.1484-9A>G	ENSP00000339883.2:n.1484-9A>G
NM_002296.3:c.1484-9A>G	NP_002287.2:n.1484-9A>G
NM_194442.2:c.1484-9A>G	NP_919424.1:n.1484-9A>G
XM_005273125.2:c.1358-9A>G	XP_005273182.1:n.1358-9A>G
XM_011544185.1:c.1484-9A>G	XP_011542487.1:n.1484-9A>G
XM_011544186.1:c.1484-189A>G	XP_011542488.1:n.1484-189A>G
XM_005273125.3:c.1358-9A>G	XP_005273182.1:n.1358-9A>G
XM_011544185.3:c.1484-9A>G	XP_011542487.1:n.1484-9A>G
XR_001737168.2:n.1507-9A>G
NM_002296.4:c.1484-9A>G MANE Select	NP_002287.2:n.1484-9A>G
NM_194442.3:c.1484-9A>G	NP_919424.1:n.1484-9A>G