Canonical Allele Identifier: CA635117083

Gene: LINC01432

Linked Data

• dbSNP Id: rs1363224863
• gnomAD v2: 20-22050493-G-T
• gnomAD v3: 20-22069855-G-T
• gnomAD v4: 20-22069855-G-T
• MyVariant Identifiers: chr20:g.22050493G>T (hg19) ; chr20:g.22069855G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069855G>T , CM000682.2:g.22069855G>T	GRCh38
NC_000020.10:g.22050493G>T , CM000682.1:g.22050493G>T	GRCh37
NC_000020.9:g.21998493G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1167G>T