Canonical Allele Identifier: CA170532284

Gene: LINC03021

Linked Data

• dbSNP Id: rs190394840
• MyVariant Identifiers: chr8:g.2649318C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649318C>G , CM000670.2:g.2649318C>G	GRCh38
NC_000008.10:g.2506835C>G , CM000670.1:g.2506835C>G	GRCh37
NC_000008.9:g.2494242C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25412G>C