Canonical Allele Identifier: CA824631235

Gene: LINC00951

Linked Data

• dbSNP Id: rs1429765931
• MyVariant Identifiers: chr6:g.40321885C>T (hg19) ; chr6:g.40354146C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354146C>T , CM000668.2:g.40354146C>T	GRCh38
NC_000006.11:g.40321885C>T , CM000668.1:g.40321885C>T	GRCh37
NC_000006.10:g.40429863C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1861G>A