Canonical Allele Identifier: CA313072780

Gene: LINC01432

Linked Data

• dbSNP Id: rs1004865734
• MyVariant Identifiers: chr20:g.22070043C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070043C>G , CM000682.2:g.22070043C>G	GRCh38
NC_000020.10:g.22050681C>G , CM000682.1:g.22050681C>G	GRCh37
NC_000020.9:g.21998681C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1355C>G