Canonical Allele Identifier: CA627271684

Gene: LINC01483

Linked Data

• dbSNP Id: rs1289781960
• gnomAD v2: 17-67850958-CATCTT-C
• MyVariant Identifiers: chr17:g.67850959_67850963del (hg19) ; chr17:g.69854818_69854822del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854820_69854824del , CM000679.2:g.69854820_69854824del	GRCh38
NC_000017.10:g.67850961_67850965del , CM000679.1:g.67850961_67850965del	GRCh37
NC_000017.9:g.65362556_65362560del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9334_363+9338del
NR_109972.1:n.363+9334_363+9338del