Canonical Allele Identifier: CA1211812088
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207933C= , CM000663.2:g.183207933C= GRCh38
NC_000001.10:g.183177068C= , CM000663.1:g.183177068C= GRCh37
NC_000001.9:g.181443691C= NCBI36
NG_007079.2:g.26670C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.132C= MANE Select ENSP00000264144.4:p.His44=
ENST00000264144.4:c.132C= ENSP00000264144.4:p.His44=
ENST00000493293.5:c.132C= ENSP00000432063.1:p.His44=
NM_005562.2:c.132C= NP_005553.2:p.His44=
NM_018891.2:c.132C= NP_061486.2:p.His44=
XM_017001273.2:c.132C= XP_016856762.1:p.His44=
NM_005562.3:c.132C= MANE Select NP_005553.2:p.His44=
NM_018891.3:c.132C= NP_061486.2:p.His44=