Canonical Allele Identifier: CA229246
Gene: ZNF674 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 10796
ClinVar RCV Id: RCV000088657
dbSNP Id: rs121918362

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46501237C>A , CM000685.2:g.46501237C>A GRCh38
NC_000023.9:g.46245616C>A NCBI36
NC_000023.10:g.46360672C>A , CM000685.1:g.46360672C>A GRCh37
NG_023376.1:g.49221G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000414387.6:c.334G>T ENSP00000428248.1:p.Glu112Ter
ENST00000523374.5:c.352G>T ENSP00000429148.1:p.Glu118Ter
NM_001039891.2:c.352G>T VV NP_001034980.1:p.Glu118Ter
NM_001146291.1:c.334G>T VV NP_001139763.1:p.Glu112Ter
NM_001190417.1:c.337G>T VV NP_001177346.1:p.Glu113Ter
XM_011543941.1:c.352G>T XP_011542243.1:p.Glu118Ter
XM_011543942.1:c.352G>T XP_011542244.1:p.Glu118Ter
XM_011543943.1:c.349G>T XP_011542245.1:p.Glu117Ter
XM_011543944.1:c.244G>T XP_011542246.1:p.Glu82Ter
XM_011543945.1:c.151G>T XP_011542247.1:p.Glu51Ter
XM_011543946.1:c.148G>T XP_011542248.1:p.Glu50Ter