Canonical Allele Identifier: CA137815799

Gene: LINC00951

Linked Data

• dbSNP Id: rs931196117
• MyVariant Identifiers: chr6:g.40321825T>A (hg19) ; chr6:g.40354086T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354086T>A , CM000668.2:g.40354086T>A	GRCh38
NC_000006.11:g.40321825T>A , CM000668.1:g.40321825T>A	GRCh37
NC_000006.10:g.40429803T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1921A>T