Canonical Allele Identifier: CA1695912375

Gene: LINC02981

Linked Data

• dbSNP Id: rs1782326570

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26442262G>A , CM000669.2:g.26442262G>A	GRCh38
NC_000007.13:g.26481882G>A , CM000669.1:g.26481882G>A	GRCh37
NC_000007.12:g.26448407G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011515671.1:c.336-18104G>A	XP_011513973.1:n.336-18104G>A
NR_148499.1:n.630+30023G>A
NR_148500.1:n.225+30023G>A
NR_148501.1:n.508+30023G>A
NR_148502.1:n.453+43241G>A
NR_148503.1:n.630+30023G>A
NR_148504.1:n.630+30023G>A