Canonical Allele Identifier: CA1009905602
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs1660169341
gnomAD v3: 1-183243082-CG-C
gnomAD v4: 1-183243082-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243085del , CM000663.2:g.183243085del GRCh38
NC_000001.10:g.183212220del , CM000663.1:g.183212220del GRCh37
NC_000001.9:g.181478843del NCBI36
NG_007079.2:g.61822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3329-62del MANE Select ENSP00000264144.4:n.3329-62del
ENST00000264144.4:c.3329-62del ENSP00000264144.4:n.3329-62del
NM_005562.2:c.3329-62del NP_005553.2:n.3329-62del
NM_005562.3:c.3329-62del MANE Select NP_005553.2:n.3329-62del
Search 100 bp 5'
Search 100 bp 3'