Canonical Allele Identifier: CA2355189674

Gene: LINC01432

Linked Data

• dbSNP Id: rs397865655

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070131_22070135del , CM000682.2:g.22070131_22070135del	GRCh38
NC_000020.10:g.22050769_22050773del , CM000682.1:g.22050769_22050773del	GRCh37
NC_000020.9:g.21998769_21998773del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1443_445+1447del