Canonical Allele Identifier: CA527259871
Gene: LAMC2 HGNC NCBI

Linked Data

gnomAD v2: 1-183176998-TG-T
gnomAD v4: 1-183207863-TG-T
MyVariant Identifiers: chr1:g.183176999del (hg19) chr1:g.183207864del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207864del , CM000663.2:g.183207864del GRCh38
NC_000001.10:g.183176999del , CM000663.1:g.183176999del GRCh37
NC_000001.9:g.181443622del NCBI36
NG_007079.2:g.26601del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.80-17del MANE Select ENSP00000264144.4:n.80-17del
ENST00000264144.4:c.80-17del ENSP00000264144.4:n.80-17del
ENST00000493293.5:c.80-17del ENSP00000432063.1:n.80-17del
NM_005562.2:c.80-17del NP_005553.2:n.80-17del
NM_018891.2:c.80-17del NP_061486.2:n.80-17del
XM_017001273.2:c.80-17del XP_016856762.1:n.80-17del
NM_005562.3:c.80-17del MANE Select NP_005553.2:n.80-17del
NM_018891.3:c.80-17del NP_061486.2:n.80-17del
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