Canonical Allele Identifier: CA742128384

Gene: LINC01432

Linked Data

• dbSNP Id: rs397865655
• gnomAD v3: 20-22070113-CTTTTTTTTT-C
• gnomAD v4: 20-22070113-CTTTTTTTTT-C
• MyVariant Identifiers: chr20:g.22050752_22050760del (hg19) ; chr20:g.22070114_22070122del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070127_22070135del , CM000682.2:g.22070127_22070135del	GRCh38
NC_000020.10:g.22050765_22050773del , CM000682.1:g.22050765_22050773del	GRCh37
NC_000020.9:g.21998765_21998773del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1439_445+1447del