Canonical Allele Identifier: CA1016142164

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982730392
• gnomAD v3: 20-22070112-T-TA
• gnomAD v4: 20-22070112-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070112_22070113insA , CM000682.2:g.22070112_22070113insA	GRCh38
NC_000020.10:g.22050750_22050751insA , CM000682.1:g.22050750_22050751insA	GRCh37
NC_000020.9:g.21998750_21998751insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1424_445+1425insA