Canonical Allele Identifier: CA824631274

Gene: LINC00951

Linked Data

• dbSNP Id: rs1207384561
• MyVariant Identifiers: chr6:g.40321916A>T (hg19) ; chr6:g.40354177A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354177A>T , CM000668.2:g.40354177A>T	GRCh38
NC_000006.11:g.40321916A>T , CM000668.1:g.40321916A>T	GRCh37
NC_000006.10:g.40429894A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1830T>A