Canonical Allele Identifier: CA2716236188
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs2117054770

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649166G>A , CM000670.2:g.2649166G>A GRCh38
NC_000008.10:g.2506683G>A , CM000670.1:g.2506683G>A GRCh37
NC_000008.9:g.2494090G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25564C>T