Canonical Allele Identifier: CA1211821105
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183232185A= , CM000663.2:g.183232185A= GRCh38
NC_000001.10:g.183201320A= , CM000663.1:g.183201320A= GRCh37
NC_000001.9:g.181467943A= NCBI36
NG_007079.2:g.50922A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.1858-2A= MANE Select ENSP00000264144.4:n.1858-2A=
ENST00000264144.4:c.1858-2A= ENSP00000264144.4:n.1858-2A=
ENST00000493293.5:c.1858-2A= ENSP00000432063.1:n.1858-2A=
NM_005562.2:c.1858-2A= NP_005553.2:n.1858-2A=
NM_018891.2:c.1858-2A= NP_061486.2:n.1858-2A=
XM_017001273.2:c.1858-2A= XP_016856762.1:n.1858-2A=
NM_005562.3:c.1858-2A= MANE Select NP_005553.2:n.1858-2A=
NM_018891.3:c.1858-2A= NP_061486.2:n.1858-2A=