Canonical Allele Identifier: CA313072748

Gene: LINC01432

Linked Data

• dbSNP Id: rs1039681141
• gnomAD v3: 20-22069762-C-T
• gnomAD v4: 20-22069762-C-T
• MyVariant Identifiers: chr20:g.22050400C>T (hg19) ; chr20:g.22069762C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069762C>T , CM000682.2:g.22069762C>T	GRCh38
NC_000020.10:g.22050400C>T , CM000682.1:g.22050400C>T	GRCh37
NC_000020.9:g.21998400C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1074C>T