Canonical Allele Identifier: CA1016141968

Gene: LINC01432

Linked Data

• dbSNP Id: rs1255792974
• gnomAD v3: 20-22069713-A-T
• gnomAD v4: 20-22069713-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22069713A>T , CM000682.2:g.22069713A>T	GRCh38
NC_000020.10:g.22050351A>T , CM000682.1:g.22050351A>T	GRCh37
NC_000020.9:g.21998351A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1025A>T