Canonical Allele Identifier: CA313072770

Gene: LINC01432

Linked Data

• dbSNP Id: rs540139928
• gnomAD v2: 20-22050567-A-G
• gnomAD v3: 20-22069929-A-G
• gnomAD v4: 20-22069929-A-G
• MyVariant Identifiers: chr20:g.22050567A>G (hg19) ; chr20:g.22069929A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069929A>G , CM000682.2:g.22069929A>G	GRCh38
NC_000020.10:g.22050567A>G , CM000682.1:g.22050567A>G	GRCh37
NC_000020.9:g.21998567A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1241A>G