Canonical Allele Identifier: CA170532295

Gene: LINC03021

Linked Data

• dbSNP Id: rs1011747458
• gnomAD v2: 8-2506898-G-A
• gnomAD v3: 8-2649381-G-A
• gnomAD v4: 8-2649381-G-A
• MyVariant Identifiers: chr8:g.2506898G>A (hg19) ; chr8:g.2649381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649381G>A , CM000670.2:g.2649381G>A	GRCh38
NC_000008.10:g.2506898G>A , CM000670.1:g.2506898G>A	GRCh37
NC_000008.9:g.2494305G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125425.1:n.238+25349C>T