Canonical Allele Identifier: CA1592773709
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756770310

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432069A>T , CM000667.2:g.154432069A>T GRCh38
NC_000005.9:g.153811629A>T , CM000667.1:g.153811629A>T GRCh37
NC_000005.8:g.153791822A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11293T>A