Canonical Allele Identifier: CA343691666
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183201409C>A (hg19) chr1:g.183232274C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183232274C>A , CM000663.2:g.183232274C>A GRCh38
NC_000001.10:g.183201409C>A , CM000663.1:g.183201409C>A GRCh37
NC_000001.9:g.181468032C>A NCBI36
NG_007079.2:g.51011C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.1945C>A MANE Select ENSP00000264144.4:p.Leu649Met
ENST00000264144.4:c.1945C>A ENSP00000264144.4:p.Leu649Met
ENST00000493293.5:c.1945C>A ENSP00000432063.1:p.Leu649Met
NM_005562.2:c.1945C>A NP_005553.2:p.Leu649Met
NM_018891.2:c.1945C>A NP_061486.2:p.Leu649Met
XM_017001273.2:c.1945C>A XP_016856762.1:p.Leu649Met
NM_005562.3:c.1945C>A MANE Select NP_005553.2:p.Leu649Met
NM_018891.3:c.1945C>A NP_061486.2:p.Leu649Met
Search 100 bp 5'
Search 100 bp 3'