Canonical Allele Identifier: CA1016142601

Gene: LINC01432

Linked Data

• dbSNP Id: rs1245705411
• gnomAD v3: 20-22070161-A-C
• gnomAD v4: 20-22070161-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070161A>C , CM000682.2:g.22070161A>C	GRCh38
NC_000020.10:g.22050799A>C , CM000682.1:g.22050799A>C	GRCh37
NC_000020.9:g.21998799A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1473A>C