Canonical Allele Identifier: CA2710564242
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2113246771

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431754G>C , CM000667.2:g.154431754G>C GRCh38
NC_000005.9:g.153811314G>C , CM000667.1:g.153811314G>C GRCh37
NC_000005.8:g.153791507G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11608C>G