Canonical Allele Identifier: CA805979222

Gene: SAP30L-AS1

Linked Data

• dbSNP Id: rs1272729911
• gnomAD v3: 5-154431894-CTA-C
• gnomAD v4: 5-154431894-CTA-C
• MyVariant Identifiers: chr5:g.153811455_153811456del (hg19) ; chr5:g.154431895_154431896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154431896_154431897del , CM000667.2:g.154431896_154431897del	GRCh38
NC_000005.9:g.153811456_153811457del , CM000667.1:g.153811456_153811457del	GRCh37
NC_000005.8:g.153791649_153791650del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_037897.1:n.204+11466_204+11467del