Canonical Allele Identifier: CA8498728

Gene: LIG3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35002629G>A , CM000679.2:g.35002629G>A	GRCh38
NC_000017.10:g.33329648G>A , CM000679.1:g.33329648G>A	GRCh37
NC_000017.9:g.30353761G>A	NCBI36
NG_029221.1:g.27132G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378526.9:c.2675-39G>A MANE Select	ENSP00000367787.3:n.2675-39G>A
ENST00000262327.9:c.2675-39G>A	ENSP00000262327.4:n.2675-39G>A
ENST00000378526.8:c.2675-39G>A	ENSP00000367787.3:n.2675-39G>A
ENST00000593099.5:n.2528-39G>A
NM_002311.4:c.2675-39G>A	NP_002302.2:n.2675-39G>A
NM_013975.3:c.2675-39G>A	NP_039269.2:n.2675-39G>A
XM_005257970.2:c.2702-39G>A	XP_005258027.1:n.2702-39G>A
XM_006721896.2:c.2702-39G>A	XP_006721959.1:n.2702-39G>A
XM_011524797.1:c.2702-39G>A	XP_011523099.1:n.2702-39G>A
XM_011524798.1:c.2675-39G>A	XP_011523100.1:n.2675-39G>A
XM_011524799.1:c.2675-39G>A	XP_011523101.1:n.2675-39G>A
XM_011524800.1:c.2702-39G>A	XP_011523102.1:n.2702-39G>A
XM_005257970.4:c.2702-39G>A	XP_005258027.1:n.2702-39G>A
XM_006721896.3:c.2702-39G>A	XP_006721959.1:n.2702-39G>A
XM_017024624.1:c.2675-39G>A	XP_016880113.1:n.2675-39G>A
NM_013975.4:c.2675-39G>A MANE Select	NP_039269.2:n.2675-39G>A
NM_002311.5:c.2675-39G>A	NP_002302.2:n.2675-39G>A