Canonical Allele Identifier: CA1592773720
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1582030374

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432085C>G , CM000667.2:g.154432085C>G GRCh38
NC_000005.9:g.153811645C>G , CM000667.1:g.153811645C>G GRCh37
NC_000005.8:g.153791838C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11277G>C