Canonical Allele Identifier: CA205878
Gene: ZNF526 HGNC NCBI

Linked Data

ClinVar Variation Id: 212683
ClinVar RCV Id: RCV000192801 RCV002517155
dbSNP Id: rs776086354
ExAC: 19:42730227 C / T
gnomAD v2: 19-42730227-C-T
gnomAD v4: 19-42226075-C-T
MyVariant Identifiers: chr19:g.42730227C>T (hg19) chr19:g.42226075C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42226075C>T , CM000681.2:g.42226075C>T GRCh38
NC_000019.9:g.42730227C>T , CM000681.1:g.42730227C>T GRCh37
NC_000019.8:g.47422067C>T NCBI36
NG_053183.1:g.10805C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710326.1:c.1672C>T ENSP00000518206.1:p.Arg558Cys
ENST00000301215.8:c.1672C>T MANE Select ENSP00000301215.2:p.Arg558Cys
ENST00000678490.1:c.93+5982G>A
ENST00000301215.7:c.1672C>T ENSP00000301215.2:p.Arg558Cys
NM_001314033.1:c.1672C>T NP_001300962.1:p.Arg558Cys
NM_133444.1:c.1672C>T NP_597701.1:p.Arg558Cys
NM_133444.2:c.1672C>T NP_597701.1:p.Arg558Cys
NM_001314033.2:c.1672C>T NP_001300962.1:p.Arg558Cys
NM_001314033.3:c.1672C>T NP_001300962.1:p.Arg558Cys
NM_133444.3:c.1672C>T MANE Select NP_597701.1:p.Arg558Cys
Search 100 bp 5'
Search 100 bp 3'