Canonical Allele Identifier: CA10608955
Gene: LAMC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293978
ClinVar RCV Id: RCV000276954
dbSNP Id: rs886045624
MyVariant Identifiers: chr1:g.183155348T>G (hg19) chr1:g.183186213T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183186213T>G , CM000663.2:g.183186213T>G GRCh38
NC_000001.10:g.183155348T>G , CM000663.1:g.183155348T>G GRCh37
NC_000001.9:g.181421971T>G NCBI36
NG_007079.2:g.4950T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005562.2:c.-140T>G NP_005553.2:n.-140T>G
NM_018891.2:c.-140T>G NP_061486.2:n.-140T>G
Search 100 bp 5'
Search 100 bp 3'