ClinGen Allele Registry
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Canonical Allele Identifier:
CA1592773669
Gene: SAP30L-AS1
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.154431973G= , CM000667.2:g.154431973G=
GRCh38
NC_000005.9:g.153811533G= , CM000667.1:g.153811533G=
GRCh37
NC_000005.8:g.153791726G=
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037897.1:n.204+11389C=
Search 100 bp 5'
Search 100 bp 3'