Canonical Allele Identifier: CA559984874
Gene: ZSWIM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474417
ClinVar RCV Id: RCV001971254 RCV003303542
dbSNP Id: rs1243690822
gnomAD v2: 5-60628160-GGCGGCGGCGGCGGGGGCAGCA-G
gnomAD v3: 5-61332333-GGCGGCGGCGGCGGGGGCAGCA-G
gnomAD v4: 5-61332333-GGCGGCGGCGGCGGGGGCAGCA-G
MyVariant Identifiers: chr5:g.60628161_60628181del (hg19) chr5:g.61332334_61332354del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.61332347_61332367del , CM000667.2:g.61332347_61332367del GRCh38
NC_000005.9:g.60628174_60628194del , CM000667.1:g.60628174_60628194del GRCh37
NC_000005.8:g.60663931_60663951del NCBI36
NG_053150.1:g.5075_5095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252744.6:c.75_95del MANE Select ENSP00000252744.5:p.Gly26_Gly32del
ENST00000252744.5:c.75_95del ENSP00000252744.5:p.Gly26_Gly32del
NM_020928.1:c.75_95del NP_065979.1:p.Gly26_Gly32del
NM_020928.2:c.75_95del MANE Select NP_065979.1:p.Gly26_Gly32del
Search 100 bp 5'
Search 100 bp 3'