Canonical Allele Identifier: CA170532297
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs762341924
gnomAD v3: 8-2649395-T-C
gnomAD v4: 8-2649395-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649395T>C , CM000670.2:g.2649395T>C GRCh38
NC_000008.10:g.2506912T>C , CM000670.1:g.2506912T>C GRCh37
NC_000008.9:g.2494319T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25335A>G