Canonical Allele Identifier: CA824631284

Gene: LINC00951

Linked Data

• dbSNP Id: rs1347332913
• MyVariant Identifiers: chr6:g.40321934G>T (hg19) ; chr6:g.40354195G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354195G>T , CM000668.2:g.40354195G>T	GRCh38
NC_000006.11:g.40321934G>T , CM000668.1:g.40321934G>T	GRCh37
NC_000006.10:g.40429912G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1812C>A