Canonical Allele Identifier: CA1592773608
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756767948

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431806T>C , CM000667.2:g.154431806T>C GRCh38
NC_000005.9:g.153811366T>C , CM000667.1:g.153811366T>C GRCh37
NC_000005.8:g.153791559T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11556A>G