Canonical Allele Identifier: CA1592773636
Gene: SAP30L-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431881A= , CM000667.2:g.154431881A= GRCh38
NC_000005.9:g.153811441A= , CM000667.1:g.153811441A= GRCh37
NC_000005.8:g.153791634A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11481T=