Canonical Allele Identifier: CA670599944

Gene: LINC01475

Linked Data

• dbSNP Id: rs1351766839
• gnomAD v3: 10-99527916-CGTTACTTAAACAT-C
• gnomAD v4: 10-99527916-CGTTACTTAAACAT-C
• MyVariant Identifiers: chr10:g.101287674_101287686del (hg19) ; chr10:g.99527917_99527929del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99527929_99527941del , CM000672.2:g.99527929_99527941del	GRCh38
NC_000010.10:g.101287686_101287698del , CM000672.1:g.101287686_101287698del	GRCh37
NC_000010.9:g.101277676_101277688del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120618.1:n.454_466del