Canonical Allele Identifier: CA579528878

Gene: LINC03021

Linked Data

• dbSNP Id: rs1245635091
• gnomAD v2: 8-2506816-T-C
• gnomAD v3: 8-2649299-T-C
• gnomAD v4: 8-2649299-T-C
• MyVariant Identifiers: chr8:g.2506816T>C (hg19) ; chr8:g.2649299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649299T>C , CM000670.2:g.2649299T>C	GRCh38
NC_000008.10:g.2506816T>C , CM000670.1:g.2506816T>C	GRCh37
NC_000008.9:g.2494223T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25431A>G