Canonical Allele Identifier: CA130069174

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs960640695
• gnomAD v3: 5-154432003-T-A
• gnomAD v4: 5-154432003-T-A
• MyVariant Identifiers: chr5:g.153811563T>A (hg19) ; chr5:g.154432003T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154432003T>A , CM000667.2:g.154432003T>A	GRCh38
NC_000005.9:g.153811563T>A , CM000667.1:g.153811563T>A	GRCh37
NC_000005.8:g.153791756T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11359A>T