Canonical Allele Identifier: CA1695912407
Gene: LINC02981 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442338_26442346delinsTAATTTGAA , CM000669.2:g.26442338_26442346delinsTAATTTGAA GRCh38
NC_000007.13:g.26481958_26481966delinsTAATTTGAA , CM000669.1:g.26481958_26481966delinsTAATTTGAA GRCh37
NC_000007.12:g.26448483_26448491delinsTAATTTGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18028_336-18020delinsTAATTTGAA XP_011513973.1:n.336-18028_336-18020delinsTAATTTGAA
NR_148499.1:n.630+30099_630+30107delinsTAATTTGAA
NR_148500.1:n.225+30099_225+30107delinsTAATTTGAA
NR_148501.1:n.508+30099_508+30107delinsTAATTTGAA
NR_148502.1:n.453+43317_453+43325delinsTAATTTGAA
NR_148503.1:n.630+30099_630+30107delinsTAATTTGAA
NR_148504.1:n.630+30099_630+30107delinsTAATTTGAA