Canonical Allele Identifier: CA15373771
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs10037670
gnomAD v2: 5-153811490-A-G
gnomAD v3: 5-154431930-A-G
gnomAD v4: 5-154431930-A-G
MyVariant Identifiers: chr5:g.153811490A>G (hg19) chr5:g.154431930A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431930A>G , CM000667.2:g.154431930A>G GRCh38
NC_000005.9:g.153811490A>G , CM000667.1:g.153811490A>G GRCh37
NC_000005.8:g.153791683A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11432T>C
Search 100 bp 5'
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