Canonical Allele Identifier: CA313072741

Gene: LINC01432

Linked Data

• dbSNP Id: rs888542670
• gnomAD v2: 20-22050327-GA-G
• gnomAD v3: 20-22069689-GA-G
• gnomAD v4: 20-22069689-GA-G
• COSMIC: COSN23291115
• MyVariant Identifiers: chr20:g.22050328del (hg19) ; chr20:g.22069690del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069697del , CM000682.2:g.22069697del	GRCh38
NC_000020.10:g.22050335del , CM000682.1:g.22050335del	GRCh37
NC_000020.9:g.21998335del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1009del