Canonical Allele Identifier: CA313072747

Gene: LINC01432

Linked Data

• dbSNP Id: rs755529571
• MyVariant Identifiers: chr20:g.22050389T>C (hg19) ; chr20:g.22069751T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069751T>C , CM000682.2:g.22069751T>C	GRCh38
NC_000020.10:g.22050389T>C , CM000682.1:g.22050389T>C	GRCh37
NC_000020.9:g.21998389T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1063T>C