Canonical Allele Identifier: CA343691708
Gene: LAMC2 HGNC NCBI

Linked Data

dbSNP Id: rs1186336421

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183232285G>C , CM000663.2:g.183232285G>C GRCh38
NC_000001.10:g.183201420G>C , CM000663.1:g.183201420G>C GRCh37
NC_000001.9:g.181468043G>C NCBI36
NG_007079.2:g.51022G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.1956G>C MANE Select ENSP00000264144.4:p.Arg652Ser
ENST00000264144.4:c.1956G>C ENSP00000264144.4:p.Arg652Ser
ENST00000493293.5:c.1956G>C ENSP00000432063.1:p.Arg652Ser
NM_005562.2:c.1956G>C NP_005553.2:p.Arg652Ser
NM_018891.2:c.1956G>C NP_061486.2:p.Arg652Ser
XM_017001273.2:c.1956G>C XP_016856762.1:p.Arg652Ser
NM_005562.3:c.1956G>C MANE Select NP_005553.2:p.Arg652Ser
NM_018891.3:c.1956G>C NP_061486.2:p.Arg652Ser