ClinGen Allele Registry
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Canonical Allele Identifier:
CA1592773631
Gene: SAP30L-AS1
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.154431873T= , CM000667.2:g.154431873T=
GRCh38
NC_000005.9:g.153811433T= , CM000667.1:g.153811433T=
GRCh37
NC_000005.8:g.153791626T=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_037897.1:n.204+11489A=
Search 100 bp 5'
Search 100 bp 3'