Canonical Allele Identifier: CA1758182894
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801086667

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649362C>T , CM000670.2:g.2649362C>T GRCh38
NC_000008.10:g.2506879C>T , CM000670.1:g.2506879C>T GRCh37
NC_000008.9:g.2494286C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25368G>A