Canonical Allele Identifier: CA1211824030
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs1660079055

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183239938A>T , CM000663.2:g.183239938A>T GRCh38
NC_000001.10:g.183209073A>T , CM000663.1:g.183209073A>T GRCh37
NC_000001.9:g.181475696A>T NCBI36
NG_007079.2:g.58675A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3070-102A>T MANE Select ENSP00000264144.4:n.3070-102A>T
ENST00000264144.4:c.3070-102A>T ENSP00000264144.4:n.3070-102A>T
ENST00000461729.1:n.438A>T
ENST00000493293.5:c.3070-102A>T ENSP00000432063.1:n.3070-102A>T
NM_005562.2:c.3070-102A>T NP_005553.2:n.3070-102A>T
NM_018891.2:c.3070-102A>T NP_061486.2:n.3070-102A>T
NM_005562.3:c.3070-102A>T MANE Select NP_005553.2:n.3070-102A>T
NM_018891.3:c.3070-102A>T NP_061486.2:n.3070-102A>T