Canonical Allele Identifier: CA343670177

Gene: LAMC2

Linked Data

• MyVariant Identifiers: chr1:g.183177159C>T (hg19) ; chr1:g.183208024C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183208024C>T , CM000663.2:g.183208024C>T	GRCh38
NC_000001.10:g.183177159C>T , CM000663.1:g.183177159C>T	GRCh37
NC_000001.9:g.181443782C>T	NCBI36
NG_007079.2:g.26761C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.223C>T MANE Select	ENSP00000264144.4:p.His75Tyr
ENST00000264144.4:c.223C>T	ENSP00000264144.4:p.His75Tyr
ENST00000493293.5:c.223C>T	ENSP00000432063.1:p.His75Tyr
NM_005562.2:c.223C>T	NP_005553.2:p.His75Tyr
NM_018891.2:c.223C>T	NP_061486.2:p.His75Tyr
XM_017001273.2:c.223C>T	XP_016856762.1:p.His75Tyr
NM_005562.3:c.223C>T MANE Select	NP_005553.2:p.His75Tyr
NM_018891.3:c.223C>T	NP_061486.2:p.His75Tyr