Canonical Allele Identifier: CA1211812100
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207951A= , CM000663.2:g.183207951A= GRCh38
NC_000001.10:g.183177086A= , CM000663.1:g.183177086A= GRCh37
NC_000001.9:g.181443709A= NCBI36
NG_007079.2:g.26688A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.150A= MANE Select ENSP00000264144.4:p.Gly50=
ENST00000264144.4:c.150A= ENSP00000264144.4:p.Gly50=
ENST00000493293.5:c.150A= ENSP00000432063.1:p.Gly50=
NM_005562.2:c.150A= NP_005553.2:p.Gly50=
NM_018891.2:c.150A= NP_061486.2:p.Gly50=
XM_017001273.2:c.150A= XP_016856762.1:p.Gly50=
NM_005562.3:c.150A= MANE Select NP_005553.2:p.Gly50=
NM_018891.3:c.150A= NP_061486.2:p.Gly50=