Canonical Allele Identifier: CA2350433850

Gene: LINC00687

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.11810079G= , CM000682.2:g.11810079G=	GRCh38
NC_000020.10:g.11790727G= , CM000682.1:g.11790727G=	GRCh37
NC_000020.9:g.11738727G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110635.1:n.432C=