Canonical Allele Identifier: CA343662580
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183212324A>C (hg19) chr1:g.183243189A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183243189A>C , CM000663.2:g.183243189A>C GRCh38
NC_000001.10:g.183212324A>C , CM000663.1:g.183212324A>C GRCh37
NC_000001.9:g.181478947A>C NCBI36
NG_007079.2:g.61926A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.3371A>C MANE Select ENSP00000264144.4:p.Glu1124Ala
ENST00000264144.4:c.3371A>C ENSP00000264144.4:p.Glu1124Ala
NM_005562.2:c.3371A>C NP_005553.2:p.Glu1124Ala
NM_005562.3:c.3371A>C MANE Select NP_005553.2:p.Glu1124Ala
Search 100 bp 5'
Search 100 bp 3'