Canonical Allele Identifier: CA1695912379
Gene: LINC02981 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442268A= , CM000669.2:g.26442268A= GRCh38
NC_000007.13:g.26481888A= , CM000669.1:g.26481888A= GRCh37
NC_000007.12:g.26448413A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18098A= XP_011513973.1:n.336-18098A=
NR_148499.1:n.630+30029A=
NR_148500.1:n.225+30029A=
NR_148501.1:n.508+30029A=
NR_148502.1:n.453+43247A=
NR_148503.1:n.630+30029A=
NR_148504.1:n.630+30029A=