Canonical Allele Identifier: CA422119610

Gene: LAMC2

Linked Data

• MyVariant Identifiers: chr1:g.183201390A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183232255A>G , CM000663.2:g.183232255A>G	GRCh38
NC_000001.10:g.183201390A>G , CM000663.1:g.183201390A>G	GRCh37
NC_000001.9:g.181468013A>G	NCBI36
NG_007079.2:g.50992A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.1926A>G MANE Select	ENSP00000264144.4:p.Gly642=
ENST00000264144.4:c.1926A>G	ENSP00000264144.4:p.Gly642=
ENST00000493293.5:c.1926A>G	ENSP00000432063.1:p.Gly642=
NM_005562.2:c.1926A>G	NP_005553.2:p.Gly642=
NM_018891.2:c.1926A>G	NP_061486.2:p.Gly642=
XM_017001273.2:c.1926A>G	XP_016856762.1:p.Gly642=
NM_005562.3:c.1926A>G MANE Select	NP_005553.2:p.Gly642=
NM_018891.3:c.1926A>G	NP_061486.2:p.Gly642=