Canonical Allele Identifier: CA1695912381
Gene: LINC02981 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442272T= , CM000669.2:g.26442272T= GRCh38
NC_000007.13:g.26481892T= , CM000669.1:g.26481892T= GRCh37
NC_000007.12:g.26448417T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011515671.1:c.336-18094T= XP_011513973.1:n.336-18094T=
NR_148499.1:n.630+30033T=
NR_148500.1:n.225+30033T=
NR_148501.1:n.508+30033T=
NR_148502.1:n.453+43251T=
NR_148503.1:n.630+30033T=
NR_148504.1:n.630+30033T=