Canonical Allele Identifier: CA343660245
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183209192C>A (hg19) chr1:g.183240057C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183240057C>A , CM000663.2:g.183240057C>A GRCh38
NC_000001.10:g.183209192C>A , CM000663.1:g.183209192C>A GRCh37
NC_000001.9:g.181475815C>A NCBI36
NG_007079.2:g.58794C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.3087C>A MANE Select ENSP00000264144.4:p.Asn1029Lys
ENST00000264144.4:c.3087C>A ENSP00000264144.4:p.Asn1029Lys
ENST00000461729.1:n.557C>A
ENST00000493293.5:c.3087C>A ENSP00000432063.1:p.Asn1029Lys
NM_005562.2:c.3087C>A NP_005553.2:p.Asn1029Lys
NM_018891.2:c.3087C>A NP_061486.2:p.Asn1029Lys
NM_005562.3:c.3087C>A MANE Select NP_005553.2:p.Asn1029Lys
NM_018891.3:c.3087C>A NP_061486.2:p.Asn1029Lys
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