Canonical Allele Identifier: CA1083165579
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756768044

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431815T>A , CM000667.2:g.154431815T>A GRCh38
NC_000005.9:g.153811375T>A , CM000667.1:g.153811375T>A GRCh37
NC_000005.8:g.153791568T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11547A>T