Canonical Allele Identifier: CA313072761

Gene: LINC01432

Linked Data

• dbSNP Id: rs971507282
• gnomAD v3: 20-22069836-A-T
• gnomAD v4: 20-22069836-A-T
• MyVariant Identifiers: chr20:g.22050474A>T (hg19) ; chr20:g.22069836A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069836A>T , CM000682.2:g.22069836A>T	GRCh38
NC_000020.10:g.22050474A>T , CM000682.1:g.22050474A>T	GRCh37
NC_000020.9:g.21998474A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1148A>T