Canonical Allele Identifier: CA13952072
Gene: ZBTB42 HGNC NCBI
gnomAD v2:
14:105269779 T / C
gnomAD v3:
14:104803442 T / C
gnomAD v4:
chr14-104803442-T-C
Joint Max Group AF 0.9040124 (NFE)
Genomes Max Group AF 0.90397032 (NFE)
Exomes Max Group AF 0.83999758 (NFE)
dbSNP:
3803300
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104803442T>C , CM000676.2:g.104803442T>C GRCh38
NC_000014.8:g.105269779T>C , CM000676.1:g.105269779T>C GRCh37
NC_000014.7:g.104340824T>C NCBI36
NG_042073.1:g.7262T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342537.8:c.*976T>C MANE Select ENSP00000409107.2:n.*976T>C
ENST00000342537.7:c.*976T>C ENSP00000409107.2:n.*976T>C
NM_001137601.1:c.*976T>C NP_001131073.1:n.*976T>C
NM_001137601.2:c.*976T>C NP_001131073.1:n.*976T>C
XM_017020911.1:c.*976T>C XP_016876400.1:n.*976T>C
NM_001137601.3:c.*976T>C MANE Select NP_001131073.1:n.*976T>C
NM_001370342.1:c.*976T>C NP_001357271.1:n.*976T>C
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