Canonical Allele Identifier: CA130068911

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs758750200
• gnomAD v2: 5-153811300-G-A
• gnomAD v3: 5-154431740-G-A
• gnomAD v4: 5-154431740-G-A
• MyVariant Identifiers: chr5:g.153811300G>A (hg19) ; chr5:g.154431740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154431740G>A , CM000667.2:g.154431740G>A	GRCh38
NC_000005.9:g.153811300G>A , CM000667.1:g.153811300G>A	GRCh37
NC_000005.8:g.153791493G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_037897.1:n.204+11622C>T