Canonical Allele Identifier: CA343669182

Gene: LAMC2

Linked Data

• MyVariant Identifiers: chr1:g.183177029T>G (hg19) ; chr1:g.183207894T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207894T>G , CM000663.2:g.183207894T>G	GRCh38
NC_000001.10:g.183177029T>G , CM000663.1:g.183177029T>G	GRCh37
NC_000001.9:g.181443652T>G	NCBI36
NG_007079.2:g.26631T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.93T>G MANE Select	ENSP00000264144.4:p.Asn31Lys
ENST00000264144.4:c.93T>G	ENSP00000264144.4:p.Asn31Lys
ENST00000493293.5:c.93T>G	ENSP00000432063.1:p.Asn31Lys
NM_005562.2:c.93T>G	NP_005553.2:p.Asn31Lys
NM_018891.2:c.93T>G	NP_061486.2:p.Asn31Lys
XM_017001273.2:c.93T>G	XP_016856762.1:p.Asn31Lys
NM_005562.3:c.93T>G MANE Select	NP_005553.2:p.Asn31Lys
NM_018891.3:c.93T>G	NP_061486.2:p.Asn31Lys