Canonical Allele Identifier: CA343662581
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183212324A>G (hg19) chr1:g.183243189A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243189A>G , CM000663.2:g.183243189A>G GRCh38
NC_000001.10:g.183212324A>G , CM000663.1:g.183212324A>G GRCh37
NC_000001.9:g.181478947A>G NCBI36
NG_007079.2:g.61926A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3371A>G MANE Select ENSP00000264144.4:p.Glu1124Gly
ENST00000264144.4:c.3371A>G ENSP00000264144.4:p.Glu1124Gly
NM_005562.2:c.3371A>G NP_005553.2:p.Glu1124Gly
NM_005562.3:c.3371A>G MANE Select NP_005553.2:p.Glu1124Gly
Search 100 bp 5'
Search 100 bp 3'