Canonical Allele Identifier: CA130069088
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1006324676
gnomAD v3: 5-154431918-G-C
gnomAD v4: 5-154431918-G-C
MyVariant Identifiers: chr5:g.153811478G>C (hg19) chr5:g.154431918G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431918G>C , CM000667.2:g.154431918G>C GRCh38
NC_000005.9:g.153811478G>C , CM000667.1:g.153811478G>C GRCh37
NC_000005.8:g.153791671G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11444C>G
Search 100 bp 5'
Search 100 bp 3'