Canonical Allele Identifier: CA343669145
Gene: LAMC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207892A>C , CM000663.2:g.183207892A>C GRCh38
NC_000001.10:g.183177027A>C , CM000663.1:g.183177027A>C GRCh37
NC_000001.9:g.181443650A>C NCBI36
NG_007079.2:g.26629A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.91A>C MANE Select ENSP00000264144.4:p.Asn31His
ENST00000264144.4:c.91A>C ENSP00000264144.4:p.Asn31His
ENST00000493293.5:c.91A>C ENSP00000432063.1:p.Asn31His
NM_005562.2:c.91A>C NP_005553.2:p.Asn31His
NM_018891.2:c.91A>C NP_061486.2:p.Asn31His
XM_017001273.2:c.91A>C XP_016856762.1:p.Asn31His
NM_005562.3:c.91A>C MANE Select NP_005553.2:p.Asn31His
NM_018891.3:c.91A>C NP_061486.2:p.Asn31His