Canonical Allele Identifier: CA2004203259
Gene: LINC02744 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119992810A= , CM000673.2:g.119992810A= GRCh38
NC_000011.9:g.119863519A= , CM000673.1:g.119863519A= GRCh37
NC_000011.8:g.119368729A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948086.1:n.576T=
XR_948087.1:n.199+1784T=
XR_948088.1:n.63T=
XR_948089.1:n.63T=
XR_948090.1:n.176+1784T=
XR_948091.1:n.177+1784T=
XR_948092.1:n.63T=
XR_948093.1:n.177+1784T=
XR_948094.1:n.175+1784T=
XR_948095.1:n.63T=
XR_948096.1:n.174+1784T=
XR_002957267.1:n.2115T=
XR_948086.2:n.668T=
XR_948087.2:n.346+1784T=
XR_948088.3:n.2118T=
XR_948089.3:n.2116T=
XR_948090.2:n.338+1784T=
XR_948091.2:n.340+1784T=
XR_948092.3:n.2117T=