Canonical Allele Identifier: CA742128403

Gene: LINC01432

Linked Data

• dbSNP Id: rs1414256570
• MyVariant Identifiers: chr20:g.22050757T>C (hg19) ; chr20:g.22070119T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070119T>C , CM000682.2:g.22070119T>C	GRCh38
NC_000020.10:g.22050757T>C , CM000682.1:g.22050757T>C	GRCh37
NC_000020.9:g.21998757T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1431T>C