Canonical Allele Identifier: CA313071470

Gene: LINC01432

Linked Data

• dbSNP Id: rs903348188
• MyVariant Identifiers: chr20:g.22039806T>C (hg19) ; chr20:g.22059168T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22059168T>C , CM000682.2:g.22059168T>C	GRCh38
NC_000020.10:g.22039806T>C , CM000682.1:g.22039806T>C	GRCh37
NC_000020.9:g.21987806T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.195+4884T>C