Canonical Allele Identifier: CA1016142508

Gene: LINC01432

Linked Data

• dbSNP Id: rs1600438781
• gnomAD v3: 20-22070143-A-G
• gnomAD v4: 20-22070143-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070143A>G , CM000682.2:g.22070143A>G	GRCh38
NC_000020.10:g.22050781A>G , CM000682.1:g.22050781A>G	GRCh37
NC_000020.9:g.21998781A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1455A>G