Canonical Allele Identifier: CA1211825283
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243190G= , CM000663.2:g.183243190G= GRCh38
NC_000001.10:g.183212325G= , CM000663.1:g.183212325G= GRCh37
NC_000001.9:g.181478948G= NCBI36
NG_007079.2:g.61927G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3372G= MANE Select ENSP00000264144.4:p.Glu1124=
ENST00000264144.4:c.3372G= ENSP00000264144.4:p.Glu1124=
NM_005562.2:c.3372G= NP_005553.2:p.Glu1124=
NM_005562.3:c.3372G= MANE Select NP_005553.2:p.Glu1124=