Canonical Allele Identifier: CA33948794
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs779631641
gnomAD v3: 1-183243084-G-A
gnomAD v4: 1-183243084-G-A
MyVariant Identifiers: chr1:g.183212219G>A (hg19) chr1:g.183243084G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243084G>A , CM000663.2:g.183243084G>A GRCh38
NC_000001.10:g.183212219G>A , CM000663.1:g.183212219G>A GRCh37
NC_000001.9:g.181478842G>A NCBI36
NG_007079.2:g.61821G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3329-63G>A MANE Select ENSP00000264144.4:n.3329-63G>A
ENST00000264144.4:c.3329-63G>A ENSP00000264144.4:n.3329-63G>A
NM_005562.2:c.3329-63G>A NP_005553.2:n.3329-63G>A
NM_005562.3:c.3329-63G>A MANE Select NP_005553.2:n.3329-63G>A
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