Canonical Allele Identifier: CA1695912398
Gene: LINC02981 HGNC NCBI

Linked Data

dbSNP Id: rs1782329552

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442311T>G , CM000669.2:g.26442311T>G GRCh38
NC_000007.13:g.26481931T>G , CM000669.1:g.26481931T>G GRCh37
NC_000007.12:g.26448456T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18055T>G XP_011513973.1:n.336-18055T>G
NR_148499.1:n.630+30072T>G
NR_148500.1:n.225+30072T>G
NR_148501.1:n.508+30072T>G
NR_148502.1:n.453+43290T>G
NR_148503.1:n.630+30072T>G
NR_148504.1:n.630+30072T>G