Canonical Allele Identifier: CA635117074

Gene: LINC01432

Linked Data

• dbSNP Id: rs1180519360
• gnomAD v2: 20-22050370-G-T
• gnomAD v3: 20-22069732-G-T
• gnomAD v4: 20-22069732-G-T
• MyVariant Identifiers: chr20:g.22050370G>T (hg19) ; chr20:g.22069732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069732G>T , CM000682.2:g.22069732G>T	GRCh38
NC_000020.10:g.22050370G>T , CM000682.1:g.22050370G>T	GRCh37
NC_000020.9:g.21998370G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.445+1044G>T