Canonical Allele Identifier: CA824631222

Gene: LINC00951

Linked Data

• dbSNP Id: rs1334538684
• MyVariant Identifiers: chr6:g.40321842C>G (hg19) ; chr6:g.40354103C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354103C>G , CM000668.2:g.40354103C>G	GRCh38
NC_000006.11:g.40321842C>G , CM000668.1:g.40321842C>G	GRCh37
NC_000006.10:g.40429820C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1904G>C