Canonical Allele Identifier: CA231677
Gene: ZNF526 HGNC NCBI

Linked Data

ClinVar Variation Id: 130830
ClinVar RCV Id: RCV000118946
dbSNP Id: rs369862002
ExAC: 19:42730040 G / A
gnomAD v2: 19-42730040-G-A
gnomAD v3: 19-42225888-G-A
gnomAD v4: 19-42225888-G-A
MyVariant Identifiers: chr19:g.42730040G>A (hg19) chr19:g.42225888G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42225888G>A , CM000681.2:g.42225888G>A GRCh38
NC_000019.9:g.42730040G>A , CM000681.1:g.42730040G>A GRCh37
NC_000019.8:g.47421880G>A NCBI36
NG_053183.1:g.10618G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710326.1:c.1485G>A ENSP00000518206.1:p.Thr495=
ENST00000301215.8:c.1485G>A MANE Select ENSP00000301215.2:p.Thr495=
ENST00000678490.1:c.93+6169C>T
ENST00000301215.7:c.1485G>A ENSP00000301215.2:p.Thr495=
NM_001314033.1:c.1485G>A NP_001300962.1:p.Thr495=
NM_133444.1:c.1485G>A NP_597701.1:p.Thr495=
NM_133444.2:c.1485G>A NP_597701.1:p.Thr495=
NM_001314033.2:c.1485G>A NP_001300962.1:p.Thr495=
NM_001314033.3:c.1485G>A NP_001300962.1:p.Thr495=
NM_133444.3:c.1485G>A MANE Select NP_597701.1:p.Thr495=
Search 100 bp 5'
Search 100 bp 3'