Canonical Allele Identifier: CA742122531

Gene: LINC01432

Linked Data

• dbSNP Id: rs1256970887
• gnomAD v3: 20-22059257-G-C
• gnomAD v4: 20-22059257-G-C
• MyVariant Identifiers: chr20:g.22039895G>C (hg19) ; chr20:g.22059257G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22059257G>C , CM000682.2:g.22059257G>C	GRCh38
NC_000020.10:g.22039895G>C , CM000682.1:g.22039895G>C	GRCh37
NC_000020.9:g.21987895G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.195+4973G>C