Canonical Allele Identifier: CA1083165571
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1756767263

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431749C>T , CM000667.2:g.154431749C>T GRCh38
NC_000005.9:g.153811309C>T , CM000667.1:g.153811309C>T GRCh37
NC_000005.8:g.153791502C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11613G>A