Canonical Allele Identifier: CA130068952

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs924348107
• gnomAD v3: 5-154431762-C-G
• gnomAD v4: 5-154431762-C-G
• MyVariant Identifiers: chr5:g.153811322C>G (hg19) ; chr5:g.154431762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154431762C>G , CM000667.2:g.154431762C>G	GRCh38
NC_000005.9:g.153811322C>G , CM000667.1:g.153811322C>G	GRCh37
NC_000005.8:g.153791515C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11600G>C