Canonical Allele Identifier: CA805979208
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1478960187

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431850A>C , CM000667.2:g.154431850A>C GRCh38
NC_000005.9:g.153811410A>C , CM000667.1:g.153811410A>C GRCh37
NC_000005.8:g.153791603A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11512T>G