Canonical Allele Identifier: CA650567391
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432007G>A , CM000667.2:g.154432007G>A GRCh38
NC_000005.9:g.153811567G>A , CM000667.1:g.153811567G>A GRCh37
NC_000005.8:g.153791760G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11355C>T