Canonical Allele Identifier: CA1109725641
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801089457
gnomAD v3: 8-2649470-T-C
gnomAD v4: 8-2649470-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649470T>C , CM000670.2:g.2649470T>C GRCh38
NC_000008.10:g.2506987T>C , CM000670.1:g.2506987T>C GRCh37
NC_000008.9:g.2494394T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125425.1:n.238+25260A>G
Search 100 bp 5'
Search 100 bp 3'