Canonical Allele Identifier: CA170532246
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs929339928
gnomAD v3: 8-2649103-A-G
gnomAD v4: 8-2649103-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649103A>G , CM000670.2:g.2649103A>G GRCh38
NC_000008.10:g.2506620A>G , CM000670.1:g.2506620A>G GRCh37
NC_000008.9:g.2494027A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25627T>C