Canonical Allele Identifier: CA130069016
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs907119787

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431856A>G , CM000667.2:g.154431856A>G GRCh38
NC_000005.9:g.153811416A>G , CM000667.1:g.153811416A>G GRCh37
NC_000005.8:g.153791609A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11506T>C