Canonical Allele Identifier: CA313072754

Gene: LINC01432

Linked Data

• dbSNP Id: rs185001906
• gnomAD v2: 20-22050440-G-A
• gnomAD v3: 20-22069802-G-A
• gnomAD v4: 20-22069802-G-A
• MyVariant Identifiers: chr20:g.22050440G>A (hg19) ; chr20:g.22069802G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069802G>A , CM000682.2:g.22069802G>A	GRCh38
NC_000020.10:g.22050440G>A , CM000682.1:g.22050440G>A	GRCh37
NC_000020.9:g.21998440G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.445+1114G>A