Canonical Allele Identifier: CA130069236
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs915664619
gnomAD v3: 5-154432113-G-T
gnomAD v4: 5-154432113-G-T
MyVariant Identifiers: chr5:g.153811673G>T (hg19) chr5:g.154432113G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432113G>T , CM000667.2:g.154432113G>T GRCh38
NC_000005.9:g.153811673G>T , CM000667.1:g.153811673G>T GRCh37
NC_000005.8:g.153791866G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11249C>A
Search 100 bp 5'
Search 100 bp 3'