Canonical Allele Identifier: CA170532289

Gene: LINC03021

Linked Data

• dbSNP Id: rs143531989
• gnomAD v3: 8-2649334-T-C
• gnomAD v4: 8-2649334-T-C
• MyVariant Identifiers: chr8:g.2506851T>C (hg19) ; chr8:g.2649334T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649334T>C , CM000670.2:g.2649334T>C	GRCh38
NC_000008.10:g.2506851T>C , CM000670.1:g.2506851T>C	GRCh37
NC_000008.9:g.2494258T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25396A>G