Canonical Allele Identifier: CA1758182933
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801089030

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649431G>C , CM000670.2:g.2649431G>C GRCh38
NC_000008.10:g.2506948G>C , CM000670.1:g.2506948G>C GRCh37
NC_000008.9:g.2494355G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25299C>G