ClinGen Allele Registry
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Canonical Allele Identifier:
CA1592773663
Gene: SAP30L-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1756769427
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.154431951C>A , CM000667.2:g.154431951C>A
GRCh38
NC_000005.9:g.153811511C>A , CM000667.1:g.153811511C>A
GRCh37
NC_000005.8:g.153791704C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037897.1:n.204+11411G>T
Search 100 bp 5'
Search 100 bp 3'