Canonical Allele Identifier: CA343669336

Gene: LAMC2

Linked Data

• MyVariant Identifiers: chr1:g.183177047T>G (hg19) ; chr1:g.183207912T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207912T>G , CM000663.2:g.183207912T>G	GRCh38
NC_000001.10:g.183177047T>G , CM000663.1:g.183177047T>G	GRCh37
NC_000001.9:g.181443670T>G	NCBI36
NG_007079.2:g.26649T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.111T>G MANE Select	ENSP00000264144.4:p.Cys37Trp
ENST00000264144.4:c.111T>G	ENSP00000264144.4:p.Cys37Trp
ENST00000493293.5:c.111T>G	ENSP00000432063.1:p.Cys37Trp
NM_005562.2:c.111T>G	NP_005553.2:p.Cys37Trp
NM_018891.2:c.111T>G	NP_061486.2:p.Cys37Trp
XM_017001273.2:c.111T>G	XP_016856762.1:p.Cys37Trp
NM_005562.3:c.111T>G MANE Select	NP_005553.2:p.Cys37Trp
NM_018891.3:c.111T>G	NP_061486.2:p.Cys37Trp