Canonical Allele Identifier: CA1758182856
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801085469

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649294A>T , CM000670.2:g.2649294A>T GRCh38
NC_000008.10:g.2506811A>T , CM000670.1:g.2506811A>T GRCh37
NC_000008.9:g.2494218A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25436T>A