Canonical Allele Identifier: CA1592773696
Gene: SAP30L-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432047T= , CM000667.2:g.154432047T= GRCh38
NC_000005.9:g.153811607T= , CM000667.1:g.153811607T= GRCh37
NC_000005.8:g.153791800T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11315A=