Canonical Allele Identifier: CA1211812092
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207939A= , CM000663.2:g.183207939A= GRCh38
NC_000001.10:g.183177074A= , CM000663.1:g.183177074A= GRCh37
NC_000001.9:g.181443697A= NCBI36
NG_007079.2:g.26676A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.138A= MANE Select ENSP00000264144.4:p.Gln46=
ENST00000264144.4:c.138A= ENSP00000264144.4:p.Gln46=
ENST00000493293.5:c.138A= ENSP00000432063.1:p.Gln46=
NM_005562.2:c.138A= NP_005553.2:p.Gln46=
NM_018891.2:c.138A= NP_061486.2:p.Gln46=
XM_017001273.2:c.138A= XP_016856762.1:p.Gln46=
NM_005562.3:c.138A= MANE Select NP_005553.2:p.Gln46=
NM_018891.3:c.138A= NP_061486.2:p.Gln46=