Canonical Allele Identifier: CA1016142426

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982730694
• gnomAD v3: 20-22070115-T-TC
• gnomAD v4: 20-22070115-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070115_22070116insC , CM000682.2:g.22070115_22070116insC	GRCh38
NC_000020.10:g.22050753_22050754insC , CM000682.1:g.22050753_22050754insC	GRCh37
NC_000020.9:g.21998753_21998754insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1427_445+1428insC