Canonical Allele Identifier: CA343691617
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183201391G>A (hg19) chr1:g.183232256G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183232256G>A , CM000663.2:g.183232256G>A GRCh38
NC_000001.10:g.183201391G>A , CM000663.1:g.183201391G>A GRCh37
NC_000001.9:g.181468014G>A NCBI36
NG_007079.2:g.50993G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.1927G>A MANE Select ENSP00000264144.4:p.Val643Ile
ENST00000264144.4:c.1927G>A ENSP00000264144.4:p.Val643Ile
ENST00000493293.5:c.1927G>A ENSP00000432063.1:p.Val643Ile
NM_005562.2:c.1927G>A NP_005553.2:p.Val643Ile
NM_018891.2:c.1927G>A NP_061486.2:p.Val643Ile
XM_017001273.2:c.1927G>A XP_016856762.1:p.Val643Ile
NM_005562.3:c.1927G>A MANE Select NP_005553.2:p.Val643Ile
NM_018891.3:c.1927G>A NP_061486.2:p.Val643Ile
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