Canonical Allele Identifier: CA2004203330

Gene: LINC02744

Linked Data

• dbSNP Id: rs1861856260

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119992902C>T , CM000673.2:g.119992902C>T	GRCh38
NC_000011.9:g.119863611C>T , CM000673.1:g.119863611C>T	GRCh37
NC_000011.8:g.119368821C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948086.1:n.484G>A
XR_948087.1:n.199+1692G>A
XR_948090.1:n.176+1692G>A
XR_948091.1:n.177+1692G>A
XR_948093.1:n.177+1692G>A
XR_948094.1:n.175+1692G>A
XR_948096.1:n.174+1692G>A
XR_002957267.1:n.2023G>A
XR_948086.2:n.576G>A
XR_948087.2:n.346+1692G>A
XR_948088.3:n.2026G>A
XR_948089.3:n.2024G>A
XR_948090.2:n.338+1692G>A
XR_948091.2:n.340+1692G>A
XR_948092.3:n.2025G>A