Canonical Allele Identifier: CA1083165627
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1582030346

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431986G>A , CM000667.2:g.154431986G>A GRCh38
NC_000005.9:g.153811546G>A , CM000667.1:g.153811546G>A GRCh37
NC_000005.8:g.153791739G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11376C>T