Canonical Allele Identifier: CA207540
Gene: ZNF526 HGNC NCBI

Linked Data

ClinVar Variation Id: 212684
ClinVar RCV Id: RCV000193807
dbSNP Id: rs749529712
ExAC: 19:42730313 G / A
gnomAD v2: 19-42730313-G-A
gnomAD v3: 19-42226161-G-A
gnomAD v4: 19-42226161-G-A
MyVariant Identifiers: chr19:g.42730313G>A (hg19) chr19:g.42226161G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42226161G>A , CM000681.2:g.42226161G>A GRCh38
NC_000019.9:g.42730313G>A , CM000681.1:g.42730313G>A GRCh37
NC_000019.8:g.47422153G>A NCBI36
NG_053183.1:g.10891G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710326.1:c.1758G>A ENSP00000518206.1:p.Ala586=
ENST00000301215.8:c.1758G>A MANE Select ENSP00000301215.2:p.Ala586=
ENST00000678490.1:c.93+5896C>T
ENST00000301215.7:c.1758G>A ENSP00000301215.2:p.Ala586=
NM_001314033.1:c.1758G>A NP_001300962.1:p.Ala586=
NM_133444.1:c.1758G>A NP_597701.1:p.Ala586=
NM_133444.2:c.1758G>A NP_597701.1:p.Ala586=
NM_001314033.2:c.1758G>A NP_001300962.1:p.Ala586=
NM_001314033.3:c.1758G>A NP_001300962.1:p.Ala586=
NM_133444.3:c.1758G>A MANE Select NP_597701.1:p.Ala586=
Search 100 bp 5'
Search 100 bp 3'