Canonical Allele Identifier: CA892149841

Gene: LAMC2

Linked Data

• dbSNP Id: rs1470638424
• MyVariant Identifiers: chr1:g.183171082A>G (hg19) ; chr1:g.183201947A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183201947A>G , CM000663.2:g.183201947A>G	GRCh38
NC_000001.10:g.183171082A>G , CM000663.1:g.183171082A>G	GRCh37
NC_000001.9:g.181437705A>G	NCBI36
NG_007079.2:g.20684A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-5934A>G MANE Select	ENSP00000264144.4:n.80-5934A>G
ENST00000264144.4:c.80-5934A>G	ENSP00000264144.4:n.80-5934A>G
ENST00000493293.5:c.80-5934A>G	ENSP00000432063.1:n.80-5934A>G
NM_005562.2:c.80-5934A>G	NP_005553.2:n.80-5934A>G
NM_018891.2:c.80-5934A>G	NP_061486.2:n.80-5934A>G
XM_017001273.2:c.80-5934A>G	XP_016856762.1:n.80-5934A>G
NM_005562.3:c.80-5934A>G MANE Select	NP_005553.2:n.80-5934A>G
NM_018891.3:c.80-5934A>G	NP_061486.2:n.80-5934A>G