Canonical Allele Identifier: CA4839463

Gene: ZFPM2

Linked Data

• ClinVar Variation Id: 260177
• ClinVar RCV Id: RCV000254101 ; RCV001668526 ; RCV002244630 ; RCV002058228
• dbSNP Id: rs3735953
• ExAC: 8:106573578 C / T
• gnomAD v2: 8-106573578-C-T
• gnomAD v3: 8-105561350-C-T
• gnomAD v4: 8-105561350-C-T
• MyVariant Identifiers: chr8:g.106573578C>T (hg19) ; chr8:g.105561350C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105561350C>T , CM000670.2:g.105561350C>T	GRCh38
NC_000008.10:g.106573578C>T , CM000670.1:g.106573578C>T	GRCh37
NC_000008.9:g.106642754C>T	NCBI36
NG_011723.1:g.247432C>T
NG_011723.2:g.247432C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.302-13C>T MANE Select	ENSP00000384179.2:n.302-13C>T
ENST00000407775.6:c.302-13C>T	ENSP00000384179.2:n.302-13C>T
ENST00000511341.6:n.1042-13C>T
ENST00000517361.1:c.-95-13C>T	ENSP00000428720.1:n.-95-13C>T
ENST00000520027.5:c.-95-13C>T	ENSP00000428149.1:n.-95-13C>T
ENST00000520492.5:c.-95-13C>T	ENSP00000430757.1:n.-95-13C>T
ENST00000524235.5:n.515-13C>T
NM_012082.3:c.302-13C>T	NP_036214.2:n.302-13C>T
XM_011516946.1:c.341-13C>T	XP_011515248.1:n.341-13C>T
XM_011516947.1:c.272-13C>T	XP_011515249.1:n.272-13C>T
XM_011516948.1:c.143-13C>T	XP_011515250.1:n.143-13C>T
XM_011516949.1:c.341-13C>T	XP_011515251.1:n.341-13C>T
NM_001362836.1:c.143-13C>T	NP_001349765.1:n.143-13C>T
NM_001362837.1:c.-95-13C>T	NP_001349766.1:n.-95-13C>T
XM_011516947.3:c.272-13C>T	XP_011515249.1:n.272-13C>T
NM_012082.4:c.302-13C>T MANE Select	NP_036214.2:n.302-13C>T
NM_001362836.2:c.143-13C>T	NP_001349765.1:n.143-13C>T
NM_001362837.2:c.-95-13C>T	NP_001349766.1:n.-95-13C>T