Canonical Allele Identifier: CA1139937847
Gene: LAMC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183239951C= , CM000663.2:g.183239951C= GRCh38
NC_000001.10:g.183209086C= , CM000663.1:g.183209086C= GRCh37
NC_000001.9:g.181475709C= NCBI36
NG_007079.2:g.58688C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3070-89C= MANE Select ENSP00000264144.4:n.3070-89C=
ENST00000264144.4:c.3070-89C= ENSP00000264144.4:n.3070-89C=
ENST00000461729.1:n.451C=
ENST00000493293.5:c.3070-89C= ENSP00000432063.1:n.3070-89C=
NM_005562.2:c.3070-89C= NP_005553.2:n.3070-89C=
NM_018891.2:c.3070-89C= NP_061486.2:n.3070-89C=
NM_005562.3:c.3070-89C= MANE Select NP_005553.2:n.3070-89C=
NM_018891.3:c.3070-89C= NP_061486.2:n.3070-89C=
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