Canonical Allele Identifier: CA1083165631
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756770089
gnomAD v3: 5-154432047-T-C
gnomAD v4: 5-154432047-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432047T>C , CM000667.2:g.154432047T>C GRCh38
NC_000005.9:g.153811607T>C , CM000667.1:g.153811607T>C GRCh37
NC_000005.8:g.153791800T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11315A>G
Search 100 bp 5'
Search 100 bp 3'