Canonical Allele Identifier: CA2716022110
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs942071792

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649488C>G , CM000670.2:g.2649488C>G GRCh38
NC_000008.10:g.2507005C>G , CM000670.1:g.2507005C>G GRCh37
NC_000008.9:g.2494412C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25242G>C