Canonical Allele Identifier: CA1133701348
Gene: ZC4H2 HGNC NCBI

Linked Data

dbSNP Id: rs1929204151
gnomAD v3: X-64921751-G-C
gnomAD v4: X-64921751-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64921751G>C , CM000685.2:g.64921751G>C GRCh38
NC_000023.10:g.64141631G>C , CM000685.1:g.64141631G>C GRCh37
NC_000023.9:g.64058356G>C NCBI36
NG_021200.1:g.59783C>G
NG_021200.2:g.117994C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476032.2:c.156+66C>G ENSP00000515193.1:n.156+66C>G
ENST00000492653.6:c.225+66C>G ENSP00000515192.1:n.225+66C>G
ENST00000703133.1:c.*799+66C>G ENSP00000515188.1:n.*799+66C>G
ENST00000703136.1:c.*183+66C>G ENSP00000515190.1:n.*183+66C>G
ENST00000374839.8:c.225+66C>G MANE Select ENSP00000363972.3:n.225+66C>G
ENST00000337990.2:c.156+66C>G ENSP00000338650.2:n.156+66C>G
ENST00000374839.7:c.225+66C>G ENSP00000363972.3:n.225+66C>G
ENST00000447788.6:c.225+66C>G ENSP00000399126.2:n.225+66C>G
ENST00000476032.1:n.466+66C>G
ENST00000488608.5:n.381+66C>G
ENST00000488831.5:n.213+66C>G
ENST00000492653.5:n.321+66C>G
NM_001178032.2:c.156+66C>G NP_001171503.1:n.156+66C>G
NM_001178033.2:c.225+66C>G NP_001171504.1:n.225+66C>G
NM_001243804.1:c.156+66C>G NP_001230733.1:n.156+66C>G
NM_018684.3:c.225+66C>G NP_061154.1:n.225+66C>G
NR_045044.1:n.636+66C>G
NM_018684.4:c.225+66C>G MANE Select NP_061154.1:n.225+66C>G
NM_001178032.3:c.156+66C>G NP_001171503.1:n.156+66C>G
NM_001243804.2:c.156+66C>G NP_001230733.1:n.156+66C>G
NR_045044.2:n.553+66C>G
NM_001178033.3:c.225+66C>G NP_001171504.1:n.225+66C>G