ClinGen Allele Registry
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Canonical Allele Identifier:
CA1083165627
Gene: SAP30L-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1582030346
gnomAD v3:
5-154431986-G-A
gnomAD v4:
5-154431986-G-A
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.154431986G>A , CM000667.2:g.154431986G>A
GRCh38
NC_000005.9:g.153811546G>A , CM000667.1:g.153811546G>A
GRCh37
NC_000005.8:g.153791739G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037897.1:n.204+11376C>T
Search 100 bp 5'
Search 100 bp 3'