Canonical Allele Identifier: CA672490395

Gene: LINC02744

Linked Data

• dbSNP Id: rs1944511
• MyVariant Identifiers: chr11:g.119863584G>T (hg19) ; chr11:g.119992875G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119992875G>T , CM000673.2:g.119992875G>T	GRCh38
NC_000011.9:g.119863584G>T , CM000673.1:g.119863584G>T	GRCh37
NC_000011.8:g.119368794G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948086.1:n.511C>A
XR_948087.1:n.199+1719C>A
XR_948090.1:n.176+1719C>A
XR_948091.1:n.177+1719C>A
XR_948093.1:n.177+1719C>A
XR_948094.1:n.175+1719C>A
XR_948096.1:n.174+1719C>A
XR_002957267.1:n.2050C>A
XR_948086.2:n.603C>A
XR_948087.2:n.346+1719C>A
XR_948088.3:n.2053C>A
XR_948089.3:n.2051C>A
XR_948090.2:n.338+1719C>A
XR_948091.2:n.340+1719C>A
XR_948092.3:n.2052C>A