Canonical Allele Identifier: CA1211825229
Gene: LAMC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243078G= , CM000663.2:g.183243078G= GRCh38
NC_000001.10:g.183212213G= , CM000663.1:g.183212213G= GRCh37
NC_000001.9:g.181478836G= NCBI36
NG_007079.2:g.61815G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3329-69G= MANE Select ENSP00000264144.4:n.3329-69G=
ENST00000264144.4:c.3329-69G= ENSP00000264144.4:n.3329-69G=
NM_005562.2:c.3329-69G= NP_005553.2:n.3329-69G=
NM_005562.3:c.3329-69G= MANE Select NP_005553.2:n.3329-69G=
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