Canonical Allele Identifier: CA1099576869

Gene: LINC02981

Linked Data

• dbSNP Id: rs1385065303

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26442231G>T , CM000669.2:g.26442231G>T	GRCh38
NC_000007.13:g.26481851G>T , CM000669.1:g.26481851G>T	GRCh37
NC_000007.12:g.26448376G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515671.1:c.336-18135G>T	XP_011513973.1:n.336-18135G>T
NR_148499.1:n.630+29992G>T
NR_148500.1:n.225+29992G>T
NR_148501.1:n.508+29992G>T
NR_148502.1:n.453+43210G>T
NR_148503.1:n.630+29992G>T
NR_148504.1:n.630+29992G>T