Canonical Allele Identifier: CA635117105

Gene: LINC01432

Linked Data

• dbSNP Id: rs1443348360
• gnomAD v2: 20-22050749-TTC-T
• gnomAD v3: 20-22070111-TTC-T
• gnomAD v4: 20-22070111-TTC-T
• MyVariant Identifiers: chr20:g.22050750_22050751del (hg19) ; chr20:g.22070112_22070113del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070113_22070114del , CM000682.2:g.22070113_22070114del	GRCh38
NC_000020.10:g.22050751_22050752del , CM000682.1:g.22050751_22050752del	GRCh37
NC_000020.9:g.21998751_21998752del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1425_445+1426del