Canonical Allele Identifier: CA137815807

Gene: LINC00951

Linked Data

• dbSNP Id: rs76957642
• MyVariant Identifiers: chr6:g.40321929A>G (hg19) ; chr6:g.40354190A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354190A>G , CM000668.2:g.40354190A>G	GRCh38
NC_000006.11:g.40321929A>G , CM000668.1:g.40321929A>G	GRCh37
NC_000006.10:g.40429907A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1817T>C