Canonical Allele Identifier: CA130069089

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs1006289197
• MyVariant Identifiers: chr5:g.153811485A>G (hg19) ; chr5:g.154431925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154431925A>G , CM000667.2:g.154431925A>G	GRCh38
NC_000005.9:g.153811485A>G , CM000667.1:g.153811485A>G	GRCh37
NC_000005.8:g.153791678A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11437T>C