Canonical Allele Identifier: CA1592773634
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs35208620

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431880C>A , CM000667.2:g.154431880C>A GRCh38
NC_000005.9:g.153811440C>A , CM000667.1:g.153811440C>A GRCh37
NC_000005.8:g.153791633C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11482G>T