Canonical Allele Identifier: CA2649468359
Gene: LAMC2 HGNC NCBI

Linked Data

gnomAD v4: 1-183243076-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243076A>T , CM000663.2:g.183243076A>T GRCh38
NC_000001.10:g.183212211A>T , CM000663.1:g.183212211A>T GRCh37
NC_000001.9:g.181478834A>T NCBI36
NG_007079.2:g.61813A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3329-71A>T MANE Select ENSP00000264144.4:n.3329-71A>T
ENST00000264144.4:c.3329-71A>T ENSP00000264144.4:n.3329-71A>T
NM_005562.2:c.3329-71A>T NP_005553.2:n.3329-71A>T
NM_005562.3:c.3329-71A>T MANE Select NP_005553.2:n.3329-71A>T
Search 100 bp 5'
Search 100 bp 3'