Canonical Allele Identifier: CA1758182941
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801089218

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649451A>C , CM000670.2:g.2649451A>C GRCh38
NC_000008.10:g.2506968A>C , CM000670.1:g.2506968A>C GRCh37
NC_000008.9:g.2494375A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25279T>G