Canonical Allele Identifier: CA2004203273
Gene: LINC02744 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119992833G= , CM000673.2:g.119992833G= GRCh38
NC_000011.9:g.119863542G= , CM000673.1:g.119863542G= GRCh37
NC_000011.8:g.119368752G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948086.1:n.553C=
XR_948087.1:n.199+1761C=
XR_948088.1:n.40C=
XR_948089.1:n.40C=
XR_948090.1:n.176+1761C=
XR_948091.1:n.177+1761C=
XR_948092.1:n.40C=
XR_948093.1:n.177+1761C=
XR_948094.1:n.175+1761C=
XR_948095.1:n.40C=
XR_948096.1:n.174+1761C=
XR_002957267.1:n.2092C=
XR_948086.2:n.645C=
XR_948087.2:n.346+1761C=
XR_948088.3:n.2095C=
XR_948089.3:n.2093C=
XR_948090.2:n.338+1761C=
XR_948091.2:n.340+1761C=
XR_948092.3:n.2094C=