Canonical Allele Identifier: CA742128211

Gene: LINC01432

Linked Data

• dbSNP Id: rs1246607077
• MyVariant Identifiers: chr20:g.22050511T>C (hg19) ; chr20:g.22069873T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069873T>C , CM000682.2:g.22069873T>C	GRCh38
NC_000020.10:g.22050511T>C , CM000682.1:g.22050511T>C	GRCh37
NC_000020.9:g.21998511T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.445+1185T>C