Canonical Allele Identifier: CA742128135

Gene: LINC01432

Linked Data

• dbSNP Id: rs1302065645
• MyVariant Identifiers: chr20:g.22050412C>T (hg19) ; chr20:g.22069774C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069774C>T , CM000682.2:g.22069774C>T	GRCh38
NC_000020.10:g.22050412C>T , CM000682.1:g.22050412C>T	GRCh37
NC_000020.9:g.21998412C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1086C>T