Canonical Allele Identifier: CA1695943917
Gene: LINC02981 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26517999A= , CM000669.2:g.26517999A= GRCh38
NC_000007.13:g.26557618A= , CM000669.1:g.26557618A= GRCh37
NC_000007.12:g.26524143A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_148499.1:n.1386-20254A=
NR_148500.1:n.981-20254A=
NR_148501.1:n.1264-20254A=
NR_148502.1:n.1209-20254A=