Canonical Allele Identifier: CA742122467

Gene: LINC01432

Linked Data

• dbSNP Id: rs1418787567
• MyVariant Identifiers: chr20:g.22039801_22039802del (hg19) ; chr20:g.22059163_22059164del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22059164_22059165del , CM000682.2:g.22059164_22059165del	GRCh38
NC_000020.10:g.22039802_22039803del , CM000682.1:g.22039802_22039803del	GRCh37
NC_000020.9:g.21987802_21987803del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.195+4880_195+4881del