Canonical Allele Identifier: CA742128223

Gene: LINC01432

Linked Data

• dbSNP Id: rs190245057
• gnomAD v3: 20-22069904-G-T
• gnomAD v4: 20-22069904-G-T
• MyVariant Identifiers: chr20:g.22050542G>T (hg19) ; chr20:g.22069904G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069904G>T , CM000682.2:g.22069904G>T	GRCh38
NC_000020.10:g.22050542G>T , CM000682.1:g.22050542G>T	GRCh37
NC_000020.9:g.21998542G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.445+1216G>T