Canonical Allele Identifier: CA422113117
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183212322G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243187G>C , CM000663.2:g.183243187G>C GRCh38
NC_000001.10:g.183212322G>C , CM000663.1:g.183212322G>C GRCh37
NC_000001.9:g.181478945G>C NCBI36
NG_007079.2:g.61924G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3369G>C MANE Select ENSP00000264144.4:p.Leu1123=
ENST00000264144.4:c.3369G>C ENSP00000264144.4:p.Leu1123=
NM_005562.2:c.3369G>C NP_005553.2:p.Leu1123=
NM_005562.3:c.3369G>C MANE Select NP_005553.2:p.Leu1123=
Search 100 bp 5'
Search 100 bp 3'