Canonical Allele Identifier: CA15941889
Gene: ZNF224 HGNC NCBI
ZNF225-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.44109508A>C
GRCh37 chr19:g.44613661A>C
gnomAD v2:
19:44613661 A / C
gnomAD v3:
19:44109508 A / C
gnomAD v4:
chr19-44109508-A-C
Joint Max Group AF 0.82246517 (NFE)
Genomes Max Group AF 0.82245997 (NFE)
Exomes Max Group AF 0.17768 (NFE)
dbSNP:
2061332
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44109508A>C , CM000681.2:g.44109508A>C GRCh38
NC_000019.9:g.44613661A>C , CM000681.1:g.44613661A>C GRCh37
NC_000019.8:g.49305501A>C NCBI36
NG_051221.1:g.20180A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684943.1:c.*1224A>C (ZNF224) ENSP00000509045.1:n.*1224A>C
ENST00000693561.1:c.*1224A>C (ZNF224) MANE Select ENSP00000508532.1:n.*1224A>C
ENST00000336976.10:c.*1224A>C (ZNF224) ENSP00000337368.5:n.*1224A>C
NR_033341.1:n.363-1171T>G (ZNF225-AS1)
XM_005259221.2:c.*1224A>C (ZNF224) XP_005259278.1:n.*1224A>C
NM_001321645.1:c.*1224A>C (ZNF224) NP_001308574.1:n.*1224A>C
NM_013398.3:c.*1224A>C (ZNF224) NP_037530.2:n.*1224A>C
XM_017027261.2:c.*1224A>C (ZNF224) XP_016882750.1:n.*1224A>C
NM_001321645.2:c.*1224A>C (ZNF224) NP_001308574.1:n.*1224A>C
NM_013398.4:c.*1224A>C (ZNF224) NP_037530.2:n.*1224A>C
NM_001321645.3:c.*1224A>C (ZNF224) MANE Select NP_001308574.1:n.*1224A>C
NM_013398.5:c.*1224A>C (ZNF224) NP_037530.2:n.*1224A>C
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