Canonical Allele Identifier: CA1592773691
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1582030353

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432032C>T , CM000667.2:g.154432032C>T GRCh38
NC_000005.9:g.153811592C>T , CM000667.1:g.153811592C>T GRCh37
NC_000005.8:g.153791785C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11330G>A