Canonical Allele Identifier: CA313072756

Gene: LINC01432

Linked Data

• dbSNP Id: rs957128813
• gnomAD v3: 20-22069813-C-T
• gnomAD v4: 20-22069813-C-T
• MyVariant Identifiers: chr20:g.22050451C>T (hg19) ; chr20:g.22069813C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069813C>T , CM000682.2:g.22069813C>T	GRCh38
NC_000020.10:g.22050451C>T , CM000682.1:g.22050451C>T	GRCh37
NC_000020.9:g.21998451C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.445+1125C>T