Canonical Allele Identifier: CA170532300

Gene: LINC03021

Linked Data

• dbSNP Id: rs1030362444
• gnomAD v2: 8-2506975-T-C
• gnomAD v3: 8-2649458-T-C
• gnomAD v4: 8-2649458-T-C
• MyVariant Identifiers: chr8:g.2506975T>C (hg19) ; chr8:g.2649458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649458T>C , CM000670.2:g.2649458T>C	GRCh38
NC_000008.10:g.2506975T>C , CM000670.1:g.2506975T>C	GRCh37
NC_000008.9:g.2494382T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125425.1:n.238+25272A>G