Canonical Allele Identifier: CA422112524
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183209189G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183240054G>C , CM000663.2:g.183240054G>C GRCh38
NC_000001.10:g.183209189G>C , CM000663.1:g.183209189G>C GRCh37
NC_000001.9:g.181475812G>C NCBI36
NG_007079.2:g.58791G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3084G>C MANE Select ENSP00000264144.4:p.Leu1028=
ENST00000264144.4:c.3084G>C ENSP00000264144.4:p.Leu1028=
ENST00000461729.1:n.554G>C
ENST00000493293.5:c.3084G>C ENSP00000432063.1:p.Leu1028=
NM_005562.2:c.3084G>C NP_005553.2:p.Leu1028=
NM_018891.2:c.3084G>C NP_061486.2:p.Leu1028=
NM_005562.3:c.3084G>C MANE Select NP_005553.2:p.Leu1028=
NM_018891.3:c.3084G>C NP_061486.2:p.Leu1028=
Search 100 bp 5'
Search 100 bp 3'