Canonical Allele Identifier: CA106818618

Gene: ZNF330

Linked Data

• dbSNP Id: rs962150371
• gnomAD v3: 4-141221624-A-G
• gnomAD v4: 4-141221624-A-G
• MyVariant Identifiers: chr4:g.142142778A>G (hg19) ; chr4:g.141221624A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221624A>G , CM000666.2:g.141221624A>G	GRCh38
NC_000004.11:g.142142778A>G , CM000666.1:g.142142778A>G	GRCh37
NC_000004.10:g.142362228A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+516A>G MANE Select	ENSP00000262990.4:n.-7+516A>G
ENST00000262990.8:c.-7+516A>G	ENSP00000262990.4:n.-7+516A>G
ENST00000503649.5:c.-7+547A>G	ENSP00000422966.1:n.-7+547A>G
ENST00000506302.1:c.-7+516A>G	ENSP00000427201.1:n.-7+516A>G
ENST00000507532.5:c.-7+516A>G	ENSP00000422574.1:n.-7+516A>G
ENST00000512738.5:c.-7+608A>G	ENSP00000422251.1:n.-7+608A>G
ENST00000512809.5:c.-7+570A>G	ENSP00000422599.1:n.-7+570A>G
ENST00000514826.5:n.222+516A>G
ENST00000515453.5:c.-7+516A>G	ENSP00000423217.1:n.-7+516A>G
NM_001292002.1:c.-116+516A>G	NP_001278931.1:n.-116+516A>G
NM_014487.5:c.-7+516A>G	NP_055302.1:n.-7+516A>G
XM_011531875.1:c.-6-742A>G	XP_011530177.1:n.-6-742A>G
XM_017008033.1:c.-6-742A>G	XP_016863522.1:n.-6-742A>G
XM_024453986.1:c.-7+547A>G	XP_024309754.1:n.-7+547A>G
NM_014487.6:c.-7+516A>G MANE Select	NP_055302.1:n.-7+516A>G
NM_001292002.2:c.-116+516A>G	NP_001278931.1:n.-116+516A>G