Canonical Allele Identifier: CA1083165581
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756768112

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431839G>A , CM000667.2:g.154431839G>A GRCh38
NC_000005.9:g.153811399G>A , CM000667.1:g.153811399G>A GRCh37
NC_000005.8:g.153791592G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11523C>T