Canonical Allele Identifier: CA1592773629
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756768420

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431860_154431861del , CM000667.2:g.154431860_154431861del GRCh38
NC_000005.9:g.153811420_153811421del , CM000667.1:g.153811420_153811421del GRCh37
NC_000005.8:g.153791613_153791614del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11501_204+11502del