Canonical Allele Identifier: CA313071231

Gene: LINC01432

Linked Data

• dbSNP Id: rs545081405
• gnomAD v3: 20-22057016-C-T
• gnomAD v4: 20-22057016-C-T
• MyVariant Identifiers: chr20:g.22037654C>T (hg19) ; chr20:g.22057016C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22057016C>T , CM000682.2:g.22057016C>T	GRCh38
NC_000020.10:g.22037654C>T , CM000682.1:g.22037654C>T	GRCh37
NC_000020.9:g.21985654C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.195+2732C>T