Canonical Allele Identifier: CA130068989

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs116672503
• gnomAD v2: 5-153811362-T-C
• gnomAD v3: 5-154431802-T-C
• gnomAD v4: 5-154431802-T-C
• MyVariant Identifiers: chr5:g.153811362T>C (hg19) ; chr5:g.154431802T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154431802T>C , CM000667.2:g.154431802T>C	GRCh38
NC_000005.9:g.153811362T>C , CM000667.1:g.153811362T>C	GRCh37
NC_000005.8:g.153791555T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11560A>G