Canonical Allele Identifier: CA1695912370
Gene: LINC02981 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442253_26442255delinsCAT , CM000669.2:g.26442253_26442255delinsCAT GRCh38
NC_000007.13:g.26481873_26481875delinsCAT , CM000669.1:g.26481873_26481875delinsCAT GRCh37
NC_000007.12:g.26448398_26448400delinsCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18113_336-18111delinsCAT XP_011513973.1:n.336-18113_336-18111delinsCAT
NR_148499.1:n.630+30014_630+30016delinsCAT
NR_148500.1:n.225+30014_225+30016delinsCAT
NR_148501.1:n.508+30014_508+30016delinsCAT
NR_148502.1:n.453+43232_453+43234delinsCAT
NR_148503.1:n.630+30014_630+30016delinsCAT
NR_148504.1:n.630+30014_630+30016delinsCAT