Canonical Allele Identifier: CA1758182960
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801089860

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649489T>G , CM000670.2:g.2649489T>G GRCh38
NC_000008.10:g.2507006T>G , CM000670.1:g.2507006T>G GRCh37
NC_000008.9:g.2494413T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25241A>C