Canonical Allele Identifier: CA422113115
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183212319A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243184A>G , CM000663.2:g.183243184A>G GRCh38
NC_000001.10:g.183212319A>G , CM000663.1:g.183212319A>G GRCh37
NC_000001.9:g.181478942A>G NCBI36
NG_007079.2:g.61921A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3366A>G MANE Select ENSP00000264144.4:p.Leu1122=
ENST00000264144.4:c.3366A>G ENSP00000264144.4:p.Leu1122=
NM_005562.2:c.3366A>G NP_005553.2:p.Leu1122=
NM_005562.3:c.3366A>G MANE Select NP_005553.2:p.Leu1122=
Search 100 bp 5'
Search 100 bp 3'