Canonical Allele Identifier: CA2545844902
Gene: LINC02744 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119992826T>C , CM000673.2:g.119992826T>C GRCh38
NC_000011.9:g.119863535T>C , CM000673.1:g.119863535T>C GRCh37
NC_000011.8:g.119368745T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948086.1:n.560A>G
XR_948087.1:n.199+1768A>G
XR_948088.1:n.47A>G
XR_948089.1:n.47A>G
XR_948090.1:n.176+1768A>G
XR_948091.1:n.177+1768A>G
XR_948092.1:n.47A>G
XR_948093.1:n.177+1768A>G
XR_948094.1:n.175+1768A>G
XR_948095.1:n.47A>G
XR_948096.1:n.174+1768A>G
XR_002957267.1:n.2099A>G
XR_948086.2:n.652A>G
XR_948087.2:n.346+1768A>G
XR_948088.3:n.2102A>G
XR_948089.3:n.2100A>G
XR_948090.2:n.338+1768A>G
XR_948091.2:n.340+1768A>G
XR_948092.3:n.2101A>G