Canonical Allele Identifier: CA1211812032
Gene: LAMC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207839T= , CM000663.2:g.183207839T= GRCh38
NC_000001.10:g.183176974T= , CM000663.1:g.183176974T= GRCh37
NC_000001.9:g.181443597T= NCBI36
NG_007079.2:g.26576T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.80-42T= MANE Select ENSP00000264144.4:n.80-42T=
ENST00000264144.4:c.80-42T= ENSP00000264144.4:n.80-42T=
ENST00000493293.5:c.80-42T= ENSP00000432063.1:n.80-42T=
NM_005562.2:c.80-42T= NP_005553.2:n.80-42T=
NM_018891.2:c.80-42T= NP_061486.2:n.80-42T=
XM_017001273.2:c.80-42T= XP_016856762.1:n.80-42T=
NM_005562.3:c.80-42T= MANE Select NP_005553.2:n.80-42T=
NM_018891.3:c.80-42T= NP_061486.2:n.80-42T=
Search 100 bp 5'
Search 100 bp 3'