Canonical Allele Identifier: CA824631227

Gene: LINC00951

Linked Data

• dbSNP Id: rs1373233104
• MyVariant Identifiers: chr6:g.40321850_40321858del (hg19) ; chr6:g.40354111_40354119del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40354111_40354119del , CM000668.2:g.40354111_40354119del	GRCh38
NC_000006.11:g.40321850_40321858del , CM000668.1:g.40321850_40321858del	GRCh37
NC_000006.10:g.40429828_40429836del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038887.1:n.1888_1896del