Canonical Allele Identifier: CA1083165629
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756769837
gnomAD v3: 5-154432014-GTAAACCAAAATC-G
gnomAD v4: 5-154432014-GTAAACCAAAATC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432015_154432026del , CM000667.2:g.154432015_154432026del GRCh38
NC_000005.9:g.153811575_153811586del , CM000667.1:g.153811575_153811586del GRCh37
NC_000005.8:g.153791768_153791779del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11336_204+11347del
Search 100 bp 5'
Search 100 bp 3'