Canonical Allele Identifier: CA635117119

Gene: LINC01432

Linked Data

• dbSNP Id: rs2122520898
• gnomAD v2: 20-22050773-TGA-T
• gnomAD v3: 20-22070135-TGA-T
• gnomAD v4: 20-22070135-TGA-T
• MyVariant Identifiers: chr20:g.22050774_22050775del (hg19) ; chr20:g.22070136_22070137del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070138_22070139del , CM000682.2:g.22070138_22070139del	GRCh38
NC_000020.10:g.22050776_22050777del , CM000682.1:g.22050776_22050777del	GRCh37
NC_000020.9:g.21998776_21998777del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1450_445+1451del