Canonical Allele Identifier: CA1083165635
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756770396
gnomAD v3: 5-154432073-C-CAATAAATAAAAATA
gnomAD v4: 5-154432073-C-CAATAAATAAAAATA
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432074_154432075insATAAATAAAAATAA , CM000667.2:g.154432074_154432075insATAAATAAAAATAA GRCh38
NC_000005.9:g.153811634_153811635insATAAATAAAAATAA , CM000667.1:g.153811634_153811635insATAAATAAAAATAA GRCh37
NC_000005.8:g.153791827_153791828insATAAATAAAAATAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11288_204+11289insTATTTTTATTTATT
Search 100 bp 5'
Search 100 bp 3'