Canonical Allele Identifier: CA805979280

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs1164268465
• MyVariant Identifiers: chr5:g.153811602A>G (hg19) ; chr5:g.154432042A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154432042A>G , CM000667.2:g.154432042A>G	GRCh38
NC_000005.9:g.153811602A>G , CM000667.1:g.153811602A>G	GRCh37
NC_000005.8:g.153791795A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11320T>C