Canonical Allele Identifier: CA850291666

Gene: LINC03021

Linked Data

• dbSNP Id: rs1207119057
• MyVariant Identifiers: chr8:g.2506812C>T (hg19) ; chr8:g.2649295C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.2649295C>T , CM000670.2:g.2649295C>T	GRCh38
NC_000008.10:g.2506812C>T , CM000670.1:g.2506812C>T	GRCh37
NC_000008.9:g.2494219C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125425.1:n.238+25435G>A