Canonical Allele Identifier: CA130069192
Gene: SAP30L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs957097551
MyVariant Identifiers: chr5:g.153811600T>A (hg19) chr5:g.154432040T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154432040T>A , CM000667.2:g.154432040T>A GRCh38
NC_000005.9:g.153811600T>A , CM000667.1:g.153811600T>A GRCh37
NC_000005.8:g.153791793T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037897.1:n.204+11322A>T
Search 100 bp 5'
Search 100 bp 3'