Canonical Allele Identifier: CA170532298

Gene: LINC03021

Linked Data

• dbSNP Id: rs976305274
• gnomAD v2: 8-2506918-A-G
• gnomAD v3: 8-2649401-A-G
• gnomAD v4: 8-2649401-A-G
• MyVariant Identifiers: chr8:g.2506918A>G (hg19) ; chr8:g.2649401A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649401A>G , CM000670.2:g.2649401A>G	GRCh38
NC_000008.10:g.2506918A>G , CM000670.1:g.2506918A>G	GRCh37
NC_000008.9:g.2494325A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125425.1:n.238+25329T>C