Canonical Allele Identifier: CA33948801
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs980373756

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243095A>T , CM000663.2:g.183243095A>T GRCh38
NC_000001.10:g.183212230A>T , CM000663.1:g.183212230A>T GRCh37
NC_000001.9:g.181478853A>T NCBI36
NG_007079.2:g.61832A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3329-52A>T MANE Select ENSP00000264144.4:n.3329-52A>T
ENST00000264144.4:c.3329-52A>T ENSP00000264144.4:n.3329-52A>T
NM_005562.2:c.3329-52A>T NP_005553.2:n.3329-52A>T
NM_005562.3:c.3329-52A>T MANE Select NP_005553.2:n.3329-52A>T