Canonical Allele Identifier: CA2004203239

Gene: LINC02744

Linked Data

• dbSNP Id: rs1861852914

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119992791A>C , CM000673.2:g.119992791A>C	GRCh38
NC_000011.9:g.119863500A>C , CM000673.1:g.119863500A>C	GRCh37
NC_000011.8:g.119368710A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948086.1:n.595T>G
XR_948087.1:n.199+1803T>G
XR_948088.1:n.82T>G
XR_948089.1:n.82T>G
XR_948090.1:n.176+1803T>G
XR_948091.1:n.177+1803T>G
XR_948092.1:n.82T>G
XR_948093.1:n.177+1803T>G
XR_948094.1:n.175+1803T>G
XR_948095.1:n.82T>G
XR_948096.1:n.174+1803T>G
XR_002957267.1:n.2134T>G
XR_948086.2:n.687T>G
XR_948087.2:n.346+1803T>G
XR_948088.3:n.2137T>G
XR_948089.3:n.2135T>G
XR_948090.2:n.338+1803T>G
XR_948091.2:n.340+1803T>G
XR_948092.3:n.2136T>G