Canonical Allele Identifier: CA14683579
Gene: ZNF627 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.11617987A>G
GRCh37 chr19:g.11728802A>G
gnomAD v2:
19:11728802 A / G
gnomAD v3:
19:11617987 A / G
gnomAD v4:
chr19-11617987-A-G
Joint Max Group AF 0.29619323 (AMR)
Genomes Max Group AF 0.29068756 (AMR)
Exomes Max Group AF 0.29688217 (AMR)
dbSNP:
4804611
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11617987A>G , CM000681.2:g.11617987A>G GRCh38
NC_000019.9:g.11728802A>G , CM000681.1:g.11728802A>G GRCh37
NC_000019.8:g.11589802A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361113.10:c.*98A>G MANE Select ENSP00000354414.4:n.*98A>G
ENST00000361113.9:c.*98A>G ENSP00000354414.4:n.*98A>G
ENST00000588174.1:c.*1269A>G ENSP00000465841.1:n.*1269A>G
NM_001290083.1:c.*98A>G NP_001277012.1:n.*98A>G
NM_001290084.1:c.*98A>G NP_001277013.1:n.*98A>G
NM_001290085.1:c.*98A>G NP_001277014.1:n.*98A>G
NM_145295.3:c.*98A>G NP_660338.1:n.*98A>G
XM_011527780.1:c.*98A>G XP_011526082.1:n.*98A>G
XM_011527780.2:c.*98A>G XP_011526082.1:n.*98A>G
NM_145295.4:c.*98A>G MANE Select NP_660338.1:n.*98A>G
NM_001290083.2:c.*98A>G NP_001277012.1:n.*98A>G
NM_001290084.2:c.*98A>G NP_001277013.1:n.*98A>G
NM_001290085.2:c.*98A>G NP_001277014.1:n.*98A>G
NM_001290084.3:c.*98A>G NP_001277013.1:n.*98A>G
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