Canonical Allele Identifier: CA130068989
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs116672503

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431802T>C , CM000667.2:g.154431802T>C GRCh38
NC_000005.9:g.153811362T>C , CM000667.1:g.153811362T>C GRCh37
NC_000005.8:g.153791555T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11560A>G