Canonical Allele Identifier: CA106818615

Gene: ZNF330

Linked Data

• dbSNP Id: rs1037651993
• gnomAD v3: 4-141221611-T-C
• gnomAD v4: 4-141221611-T-C
• MyVariant Identifiers: chr4:g.142142765T>C (hg19) ; chr4:g.141221611T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221611T>C , CM000666.2:g.141221611T>C	GRCh38
NC_000004.11:g.142142765T>C , CM000666.1:g.142142765T>C	GRCh37
NC_000004.10:g.142362215T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+503T>C MANE Select	ENSP00000262990.4:n.-7+503T>C
ENST00000262990.8:c.-7+503T>C	ENSP00000262990.4:n.-7+503T>C
ENST00000503649.5:c.-7+534T>C	ENSP00000422966.1:n.-7+534T>C
ENST00000506302.1:c.-7+503T>C	ENSP00000427201.1:n.-7+503T>C
ENST00000507532.5:c.-7+503T>C	ENSP00000422574.1:n.-7+503T>C
ENST00000512738.5:c.-7+595T>C	ENSP00000422251.1:n.-7+595T>C
ENST00000512809.5:c.-7+557T>C	ENSP00000422599.1:n.-7+557T>C
ENST00000514826.5:n.222+503T>C
ENST00000515453.5:c.-7+503T>C	ENSP00000423217.1:n.-7+503T>C
NM_001292002.1:c.-116+503T>C	NP_001278931.1:n.-116+503T>C
NM_014487.5:c.-7+503T>C	NP_055302.1:n.-7+503T>C
XM_011531875.1:c.-6-755T>C	XP_011530177.1:n.-6-755T>C
XM_017008033.1:c.-6-755T>C	XP_016863522.1:n.-6-755T>C
XM_024453986.1:c.-7+534T>C	XP_024309754.1:n.-7+534T>C
NM_014487.6:c.-7+503T>C MANE Select	NP_055302.1:n.-7+503T>C
NM_001292002.2:c.-116+503T>C	NP_001278931.1:n.-116+503T>C