Canonical Allele Identifier: CA170532282

Gene: LINC03021

Linked Data

• dbSNP Id: rs908401847
• gnomAD v2: 8-2506822-C-A
• gnomAD v3: 8-2649305-C-A
• gnomAD v4: 8-2649305-C-A
• MyVariant Identifiers: chr8:g.2506822C>A (hg19) ; chr8:g.2649305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649305C>A , CM000670.2:g.2649305C>A	GRCh38
NC_000008.10:g.2506822C>A , CM000670.1:g.2506822C>A	GRCh37
NC_000008.9:g.2494229C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25425G>T