Canonical Allele Identifier: CA1592773695
Gene: SAP30L-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432042A= , CM000667.2:g.154432042A= GRCh38
NC_000005.9:g.153811602A= , CM000667.1:g.153811602A= GRCh37
NC_000005.8:g.153791795A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11320T=