Canonical Allele Identifier: CA672490385

Gene: LINC02744

Linked Data

• dbSNP Id: rs1370596529
• MyVariant Identifiers: chr11:g.119863550C>G (hg19) ; chr11:g.119992841C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119992841C>G , CM000673.2:g.119992841C>G	GRCh38
NC_000011.9:g.119863550C>G , CM000673.1:g.119863550C>G	GRCh37
NC_000011.8:g.119368760C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948086.1:n.545G>C
XR_948087.1:n.199+1753G>C
XR_948088.1:n.32G>C
XR_948089.1:n.32G>C
XR_948090.1:n.176+1753G>C
XR_948091.1:n.177+1753G>C
XR_948092.1:n.32G>C
XR_948093.1:n.177+1753G>C
XR_948094.1:n.175+1753G>C
XR_948095.1:n.32G>C
XR_948096.1:n.174+1753G>C
XR_002957267.1:n.2084G>C
XR_948086.2:n.637G>C
XR_948087.2:n.346+1753G>C
XR_948088.3:n.2087G>C
XR_948089.3:n.2085G>C
XR_948090.2:n.338+1753G>C
XR_948091.2:n.340+1753G>C
XR_948092.3:n.2086G>C