Canonical Allele Identifier: CA343669259
Gene: LAMC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.183177037C>A (hg19) chr1:g.183207902C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207902C>A , CM000663.2:g.183207902C>A GRCh38
NC_000001.10:g.183177037C>A , CM000663.1:g.183177037C>A GRCh37
NC_000001.9:g.181443660C>A NCBI36
NG_007079.2:g.26639C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.101C>A MANE Select ENSP00000264144.4:p.Ser34Tyr
ENST00000264144.4:c.101C>A ENSP00000264144.4:p.Ser34Tyr
ENST00000493293.5:c.101C>A ENSP00000432063.1:p.Ser34Tyr
NM_005562.2:c.101C>A NP_005553.2:p.Ser34Tyr
NM_018891.2:c.101C>A NP_061486.2:p.Ser34Tyr
XM_017001273.2:c.101C>A XP_016856762.1:p.Ser34Tyr
NM_005562.3:c.101C>A MANE Select NP_005553.2:p.Ser34Tyr
NM_018891.3:c.101C>A NP_061486.2:p.Ser34Tyr
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