Canonical Allele Identifier: CA742121500

Gene: LINC01432

Linked Data

• dbSNP Id: rs1422489807
• MyVariant Identifiers: chr20:g.22037686G>T (hg19) ; chr20:g.22057048G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22057048G>T , CM000682.2:g.22057048G>T	GRCh38
NC_000020.10:g.22037686G>T , CM000682.1:g.22037686G>T	GRCh37
NC_000020.9:g.21985686G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.195+2764G>T