Canonical Allele Identifier: CA170532258

Gene: LINC03021

Linked Data

• dbSNP Id: rs111870025
• gnomAD v2: 8-2506715-G-C
• gnomAD v3: 8-2649198-G-C
• gnomAD v4: 8-2649198-G-C
• MyVariant Identifiers: chr8:g.2506715G>C (hg19) ; chr8:g.2649198G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649198G>C , CM000670.2:g.2649198G>C	GRCh38
NC_000008.10:g.2506715G>C , CM000670.1:g.2506715G>C	GRCh37
NC_000008.9:g.2494122G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25532C>G