Canonical Allele Identifier: CA130069067

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs889265040
• gnomAD v3: 5-154431906-C-T
• gnomAD v4: 5-154431906-C-T
• MyVariant Identifiers: chr5:g.153811466C>T (hg19) ; chr5:g.154431906C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154431906C>T , CM000667.2:g.154431906C>T	GRCh38
NC_000005.9:g.153811466C>T , CM000667.1:g.153811466C>T	GRCh37
NC_000005.8:g.153791659C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11456G>A