Canonical Allele Identifier: CA1592773649
Gene: SAP30L-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431906C= , CM000667.2:g.154431906C= GRCh38
NC_000005.9:g.153811466C= , CM000667.1:g.153811466C= GRCh37
NC_000005.8:g.153791659C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11456G=