Canonical Allele Identifier: CA877268236

Gene: ZC4H2

Linked Data

• dbSNP Id: rs1336034370
• gnomAD v4: X-64917742-A-G
• MyVariant Identifiers: chrX:g.64137622A>G (hg19) ; chrX:g.64917742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917742A>G , CM000685.2:g.64917742A>G	GRCh38
NC_000023.10:g.64137622A>G , CM000685.1:g.64137622A>G	GRCh37
NC_000023.9:g.64054347A>G	NCBI36
NG_021200.1:g.63792T>C
NG_021200.2:g.122003T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703133.1:c.*1290T>C	ENSP00000515188.1:n.*1290T>C
ENST00000703136.1:c.*674T>C	ENSP00000515190.1:n.*674T>C
ENST00000374839.8:c.*41T>C MANE Select	ENSP00000363972.3:n.*41T>C
ENST00000337990.2:c.*41T>C	ENSP00000338650.2:n.*41T>C
ENST00000374839.7:c.*41T>C	ENSP00000363972.3:n.*41T>C
ENST00000447788.6:c.*22T>C	ENSP00000399126.2:n.*22T>C
ENST00000488406.1:n.236T>C
ENST00000488608.5:n.2893T>C
NM_001178032.2:c.*41T>C	NP_001171503.1:n.*41T>C
NM_001178033.2:c.*22T>C	NP_001171504.1:n.*22T>C
NM_001243804.1:c.*41T>C	NP_001230733.1:n.*41T>C
NM_018684.3:c.*41T>C	NP_061154.1:n.*41T>C
NR_045044.1:n.1127T>C
NM_018684.4:c.*41T>C MANE Select	NP_061154.1:n.*41T>C
NM_001178032.3:c.*41T>C	NP_001171503.1:n.*41T>C
NM_001243804.2:c.*41T>C	NP_001230733.1:n.*41T>C
NR_045044.2:n.1044T>C
NM_001178033.3:c.*22T>C	NP_001171504.1:n.*22T>C