Canonical Allele Identifier: CA1109725661
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs950594477
gnomAD v3: 8-2649495-C-G
gnomAD v4: 8-2649495-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649495C>G , CM000670.2:g.2649495C>G GRCh38
NC_000008.10:g.2507012C>G , CM000670.1:g.2507012C>G GRCh37
NC_000008.9:g.2494419C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25235G>C