Canonical Allele Identifier: CA805979163
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1437783334
MyVariant Identifiers: chr5:g.153811337C>T (hg19) chr5:g.154431777C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154431777C>T , CM000667.2:g.154431777C>T GRCh38
NC_000005.9:g.153811337C>T , CM000667.1:g.153811337C>T GRCh37
NC_000005.8:g.153791530C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037897.1:n.204+11585G>A
Search 100 bp 5'
Search 100 bp 3'