Canonical Allele Identifier: CA850291720
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1225839606
MyVariant Identifiers: chr8:g.2506921del (hg19) chr8:g.2649404del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649405del , CM000670.2:g.2649405del GRCh38
NC_000008.10:g.2506922del , CM000670.1:g.2506922del GRCh37
NC_000008.9:g.2494329del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25326del
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