Canonical Allele Identifier: CA850291679

Gene: LINC03021

Linked Data

• dbSNP Id: rs948606280
• MyVariant Identifiers: chr8:g.2506841G>A (hg19) ; chr8:g.2649324G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649324G>A , CM000670.2:g.2649324G>A	GRCh38
NC_000008.10:g.2506841G>A , CM000670.1:g.2506841G>A	GRCh37
NC_000008.9:g.2494248G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25406C>T