Canonical Allele Identifier: CA1109725417
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801083390
gnomAD v3: 8-2649160-T-A
gnomAD v4: 8-2649160-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649160T>A , CM000670.2:g.2649160T>A GRCh38
NC_000008.10:g.2506677T>A , CM000670.1:g.2506677T>A GRCh37
NC_000008.9:g.2494084T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25570A>T