Canonical Allele Identifier: CA788151351

Gene: ZNF330

Linked Data

• dbSNP Id: rs537556637
• gnomAD v3: 4-141221441-C-T
• gnomAD v4: 4-141221441-C-T
• MyVariant Identifiers: chr4:g.142142595C>T (hg19) ; chr4:g.141221441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221441C>T , CM000666.2:g.141221441C>T	GRCh38
NC_000004.11:g.142142595C>T , CM000666.1:g.142142595C>T	GRCh37
NC_000004.10:g.142362045C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262990.9:c.-7+333C>T MANE Select	ENSP00000262990.4:n.-7+333C>T
ENST00000262990.8:c.-7+333C>T	ENSP00000262990.4:n.-7+333C>T
ENST00000503649.5:c.-7+364C>T	ENSP00000422966.1:n.-7+364C>T
ENST00000506302.1:c.-7+333C>T	ENSP00000427201.1:n.-7+333C>T
ENST00000507532.5:c.-7+333C>T	ENSP00000422574.1:n.-7+333C>T
ENST00000512738.5:c.-7+425C>T	ENSP00000422251.1:n.-7+425C>T
ENST00000512809.5:c.-7+387C>T	ENSP00000422599.1:n.-7+387C>T
ENST00000514826.5:n.222+333C>T
ENST00000515453.5:c.-7+333C>T	ENSP00000423217.1:n.-7+333C>T
NM_001292002.1:c.-116+333C>T	NP_001278931.1:n.-116+333C>T
NM_014487.5:c.-7+333C>T	NP_055302.1:n.-7+333C>T
XM_011531875.1:c.-7+881C>T	XP_011530177.1:n.-7+881C>T
XM_017008033.1:c.-7+782C>T	XP_016863522.1:n.-7+782C>T
XM_024453986.1:c.-7+364C>T	XP_024309754.1:n.-7+364C>T
NM_014487.6:c.-7+333C>T MANE Select	NP_055302.1:n.-7+333C>T
NM_001292002.2:c.-116+333C>T	NP_001278931.1:n.-116+333C>T