Canonical Allele Identifier: CA130069222

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs745418401
• MyVariant Identifiers: chr5:g.153811650T>C (hg19) ; chr5:g.154432090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154432090T>C , CM000667.2:g.154432090T>C	GRCh38
NC_000005.9:g.153811650T>C , CM000667.1:g.153811650T>C	GRCh37
NC_000005.8:g.153791843T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11272A>G