Canonical Allele Identifier: CA1009905607
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs1660169597
gnomAD v3: 1-183243094-G-A
gnomAD v4: 1-183243094-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243094G>A , CM000663.2:g.183243094G>A GRCh38
NC_000001.10:g.183212229G>A , CM000663.1:g.183212229G>A GRCh37
NC_000001.9:g.181478852G>A NCBI36
NG_007079.2:g.61831G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3329-53G>A MANE Select ENSP00000264144.4:n.3329-53G>A
ENST00000264144.4:c.3329-53G>A ENSP00000264144.4:n.3329-53G>A
NM_005562.2:c.3329-53G>A NP_005553.2:n.3329-53G>A
NM_005562.3:c.3329-53G>A MANE Select NP_005553.2:n.3329-53G>A
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