Canonical Allele Identifier: CA742128280

Gene: LINC01432

Linked Data

• dbSNP Id: rs1433888691
• MyVariant Identifiers: chr20:g.22050672A>G (hg19) ; chr20:g.22070034A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070034A>G , CM000682.2:g.22070034A>G	GRCh38
NC_000020.10:g.22050672A>G , CM000682.1:g.22050672A>G	GRCh37
NC_000020.9:g.21998672A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1346A>G