Canonical Allele Identifier: CA343660191

Gene: LAMC2

Linked Data

• MyVariant Identifiers: chr1:g.183209181G>T (hg19) ; chr1:g.183240046G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183240046G>T , CM000663.2:g.183240046G>T	GRCh38
NC_000001.10:g.183209181G>T , CM000663.1:g.183209181G>T	GRCh37
NC_000001.9:g.181475804G>T	NCBI36
NG_007079.2:g.58783G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.3076G>T MANE Select	ENSP00000264144.4:p.Gly1026Trp
ENST00000264144.4:c.3076G>T	ENSP00000264144.4:p.Gly1026Trp
ENST00000461729.1:n.546G>T
ENST00000493293.5:c.3076G>T	ENSP00000432063.1:p.Gly1026Trp
NM_005562.2:c.3076G>T	NP_005553.2:p.Gly1026Trp
NM_018891.2:c.3076G>T	NP_061486.2:p.Gly1026Trp
NM_005562.3:c.3076G>T MANE Select	NP_005553.2:p.Gly1026Trp
NM_018891.3:c.3076G>T	NP_061486.2:p.Gly1026Trp