Canonical Allele Identifier: CA1109725608
Gene: LINC03021 HGNC NCBI

Linked Data

dbSNP Id: rs1801088106
gnomAD v3: 8-2649372-C-T
gnomAD v4: 8-2649372-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2649372C>T , CM000670.2:g.2649372C>T GRCh38
NC_000008.10:g.2506889C>T , CM000670.1:g.2506889C>T GRCh37
NC_000008.9:g.2494296C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125425.1:n.238+25358G>A
Search 100 bp 5'
Search 100 bp 3'