Canonical Allele Identifier: CA9470692

Gene: ZNF526 GSK3A

Linked Data

• ClinVar Variation Id: 437390
• ClinVar RCV Id: RCV000501020 ; RCV002524351 ; RCV003159127
• dbSNP Id: rs143303371
• ExAC: 19:42730536 G / A
• gnomAD v2: 19-42730536-G-A
• gnomAD v3: 19-42226384-G-A
• gnomAD v4: 19-42226384-G-A
• MyVariant Identifiers: chr19:g.42730536G>A (hg19) ; chr19:g.42226384G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42226384G>A , CM000681.2:g.42226384G>A	GRCh38
NC_000019.9:g.42730536G>A , CM000681.1:g.42730536G>A	GRCh37
NC_000019.8:g.47422376G>A	NCBI36
NG_053183.1:g.11114G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710326.1:c.1981G>A (ZNF526)	ENSP00000518206.1:p.Gly661Arg
ENST00000301215.8:c.1981G>A (ZNF526) MANE Select	ENSP00000301215.2:p.Gly661Arg
ENST00000677025.1:c.131C>T (GSK3A)
ENST00000678490.1:c.93+5673C>T
ENST00000301215.7:c.1981G>A (ZNF526)	ENSP00000301215.2:p.Gly661Arg
NM_001314033.1:c.1981G>A (ZNF526)	NP_001300962.1:p.Gly661Arg
NM_133444.1:c.1981G>A (ZNF526)	NP_597701.1:p.Gly661Arg
NM_133444.2:c.1981G>A (ZNF526)	NP_597701.1:p.Gly661Arg
NM_001314033.2:c.1981G>A (ZNF526)	NP_001300962.1:p.Gly661Arg
NM_001314033.3:c.1981G>A (ZNF526)	NP_001300962.1:p.Gly661Arg
NM_133444.3:c.1981G>A (ZNF526) MANE Select	NP_597701.1:p.Gly661Arg