Canonical Allele Identifier: CA850291798
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1247068643

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649579_2649580del , CM000670.2:g.2649579_2649580del GRCh38
NC_000008.10:g.2507096_2507097del , CM000670.1:g.2507096_2507097del GRCh37
NC_000008.9:g.2494503_2494504del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25153_238+25154del