Canonical Allele Identifier: CA1695912351
Gene: LINC02981 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26442176_26442177delinsAG , CM000669.2:g.26442176_26442177delinsAG GRCh38
NC_000007.13:g.26481796_26481797delinsAG , CM000669.1:g.26481796_26481797delinsAG GRCh37
NC_000007.12:g.26448321_26448322delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011515671.1:c.336-18190_336-18189delinsAG XP_011513973.1:n.336-18190_336-18189delinsAG
NR_148499.1:n.630+29937_630+29938delinsAG
NR_148500.1:n.225+29937_225+29938delinsAG
NR_148501.1:n.508+29937_508+29938delinsAG
NR_148502.1:n.453+43155_453+43156delinsAG
NR_148503.1:n.630+29937_630+29938delinsAG
NR_148504.1:n.630+29937_630+29938delinsAG