Canonical Allele Identifier: CA14937734
Gene: ZNRF3 HGNC NCBI
MyVariant.info:
GRCh38 chr22:g.29055683A>G
GRCh37 chr22:g.29451671A>G
gnomAD v2:
22:29451671 A / G
gnomAD v3:
22:29055683 A / G
gnomAD v4:
chr22-29055683-A-G
Joint Max Group AF 0.55929711 (SAS)
Genomes Max Group AF 0.55929711 (SAS)
Exomes Max Group AF 0.31104785 (NFE)
dbSNP:
4823006
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29055683A>G , CM000684.2:g.29055683A>G GRCh38
NC_000022.10:g.29451671A>G , CM000684.1:g.29451671A>G GRCh37
NC_000022.9:g.27781671A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000544604.7:c.*2061A>G MANE Select ENSP00000443824.2:n.*2061A>G
ENST00000544604.6:c.*2061A>G ENSP00000443824.2:n.*2061A>G
NM_001206998.1:c.4872A>G NP_001193927.1:n.4872A>G
NM_032173.3:c.*2061A>G NP_115549.2:n.*2061A>G
XM_005261773.2:c.*2061A>G XP_005261830.1:n.*2061A>G
XM_011530434.1:c.*2061A>G XP_011528736.1:n.*2061A>G
XM_011530435.1:c.*2061A>G XP_011528737.1:n.*2061A>G
XM_011530436.1:c.*2061A>G XP_011528738.1:n.*2061A>G
XM_011530437.1:c.*2061A>G XP_011528739.1:n.*2061A>G
XM_011530438.1:c.*2061A>G XP_011528740.1:n.*2061A>G
XM_011530439.1:c.*2061A>G XP_011528741.1:n.*2061A>G
XM_011530440.1:c.*2061A>G XP_011528742.1:n.*2061A>G
XM_011530441.1:c.*2061A>G XP_011528743.1:n.*2061A>G
XM_011530435.2:c.*2061A>G XP_011528737.1:n.*2061A>G
XM_011530436.3:c.*2061A>G XP_011528738.1:n.*2061A>G
XM_011530438.2:c.*2061A>G XP_011528740.1:n.*2061A>G
XM_017028990.1:c.*2061A>G XP_016884479.1:n.*2061A>G
XM_024452286.1:c.*2061A>G XP_024308054.1:n.*2061A>G
NM_001206998.2:c.*2061A>G MANE Select NP_001193927.1:n.*2061A>G
NM_032173.4:c.*2061A>G NP_115549.2:n.*2061A>G
Search 100 bp 5'
Search 100 bp 3'