Canonical Allele Identifier: CA2649468371
Gene: LAMC2 HGNC NCBI

Linked Data

gnomAD v4: 1-183243091-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243091A>G , CM000663.2:g.183243091A>G GRCh38
NC_000001.10:g.183212226A>G , CM000663.1:g.183212226A>G GRCh37
NC_000001.9:g.181478849A>G NCBI36
NG_007079.2:g.61828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3329-56A>G MANE Select ENSP00000264144.4:n.3329-56A>G
ENST00000264144.4:c.3329-56A>G ENSP00000264144.4:n.3329-56A>G
NM_005562.2:c.3329-56A>G NP_005553.2:n.3329-56A>G
NM_005562.3:c.3329-56A>G MANE Select NP_005553.2:n.3329-56A>G
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