Canonical Allele Identifier: CA1083165630
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756769979
gnomAD v3: 5-154432031-AC-A
gnomAD v4: 5-154432031-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432032del , CM000667.2:g.154432032del GRCh38
NC_000005.9:g.153811592del , CM000667.1:g.153811592del GRCh37
NC_000005.8:g.153791785del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11330del
Search 100 bp 5'
Search 100 bp 3'