Canonical Allele Identifier: CA204077

Gene: ZNF174

Linked Data

• ClinVar Variation Id: 207844
• ClinVar RCV Id: RCV000190137
• dbSNP Id: rs761098156
• ExAC: 16:3458899 C / T
• gnomAD v2: 16-3458899-C-T
• gnomAD v4: 16-3408899-C-T
• MyVariant Identifiers: chr16:g.3458899C>T (hg19) ; chr16:g.3408899C>T (hg38)
• PubMed: PMID:26132555

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3408899C>T , CM000678.2:g.3408899C>T	GRCh38
NC_000016.9:g.3458899C>T , CM000678.1:g.3458899C>T	GRCh37
NC_000016.8:g.3398900C>T	NCBI36
NG_053015.1:g.12710C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000268655.5:c.1204C>T MANE Select	ENSP00000268655.4:p.Arg402Ter
ENST00000268655.4:c.1204C>T	ENSP00000268655.4:p.Arg402Ter
ENST00000571936.5:c.1204C>T	ENSP00000460397.1:p.Arg402Ter
ENST00000575785.2:c.211+4251C>T	ENSP00000477472.1:n.211+4251C>T
NM_003450.2:c.1204C>T	NP_003441.1:p.Arg402Ter
XM_011522649.1:c.1204C>T	XP_011520951.1:p.Arg402Ter
XM_011522650.1:c.625+4251C>T	XP_011520952.1:n.625+4251C>T
XM_011522651.1:c.625+4251C>T	XP_011520953.1:n.625+4251C>T
NM_001347868.1:c.1204C>T	NP_001334797.1:p.Arg402Ter
NM_003450.3:c.1204C>T MANE Select	NP_003441.1:p.Arg402Ter
NM_001347868.2:c.1204C>T	NP_001334797.1:p.Arg402Ter