Canonical Allele Identifier: CA1016142028

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982723310
• gnomAD v3: 20-22069833-T-C
• gnomAD v4: 20-22069833-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069833T>C , CM000682.2:g.22069833T>C	GRCh38
NC_000020.10:g.22050471T>C , CM000682.1:g.22050471T>C	GRCh37
NC_000020.9:g.21998471T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.445+1145T>C