Canonical Allele Identifier: CA313072740

Gene: LINC01432

Linked Data

• dbSNP Id: rs950787146
• MyVariant Identifiers: chr20:g.22069660G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069660G>C , CM000682.2:g.22069660G>C	GRCh38
NC_000020.10:g.22050298G>C , CM000682.1:g.22050298G>C	GRCh37
NC_000020.9:g.21998298G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+972G>C