Canonical Allele Identifier: CA1109725625
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801088677
gnomAD v3: 8-2649405-G-C
gnomAD v4: 8-2649405-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649405G>C , CM000670.2:g.2649405G>C GRCh38
NC_000008.10:g.2506922G>C , CM000670.1:g.2506922G>C GRCh37
NC_000008.9:g.2494329G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25325C>G