Canonical Allele Identifier: CA130068941
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs978264038

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431758G>A , CM000667.2:g.154431758G>A GRCh38
NC_000005.9:g.153811318G>A , CM000667.1:g.153811318G>A GRCh37
NC_000005.8:g.153791511G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11604C>T