Canonical Allele Identifier: CA2713996787

Gene: LINC02981

Linked Data

• dbSNP Id: rs2128044230

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26442269G>C , CM000669.2:g.26442269G>C	GRCh38
NC_000007.13:g.26481889G>C , CM000669.1:g.26481889G>C	GRCh37
NC_000007.12:g.26448414G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011515671.1:c.336-18097G>C	XP_011513973.1:n.336-18097G>C
NR_148499.1:n.630+30030G>C
NR_148500.1:n.225+30030G>C
NR_148501.1:n.508+30030G>C
NR_148502.1:n.453+43248G>C
NR_148503.1:n.630+30030G>C
NR_148504.1:n.630+30030G>C