Canonical Allele Identifier: CA2355189483

Gene: LINC01432

Linked Data

• dbSNP Id: rs1039681141
• gnomAD v3: 20-22069762-C-G
• gnomAD v4: 20-22069762-C-G

Genomic Alleles

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

Transcript Alleles

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