Canonical Allele Identifier: CA824631228

Gene: LINC00951

Linked Data

• dbSNP Id: rs1170002554
• MyVariant Identifiers: chr6:g.40321860T>A (hg19) ; chr6:g.40354121T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354121T>A , CM000668.2:g.40354121T>A	GRCh38
NC_000006.11:g.40321860T>A , CM000668.1:g.40321860T>A	GRCh37
NC_000006.10:g.40429838T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1886A>T