Canonical Allele Identifier: CA462650096

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 1516718
• ClinVar RCV Id: RCV002040912
• dbSNP Id: rs1186450406
• gnomAD v2: 8-106813930-C-T
• gnomAD v4: 8-105801702-C-T
• MyVariant Identifiers: chr8:g.106813930C>T (hg19) ; chr8:g.105801702C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801702C>T , CM000670.2:g.105801702C>T	GRCh38
NC_000008.10:g.106813930C>T , CM000670.1:g.106813930C>T	GRCh37
NC_000008.9:g.106883106C>T	NCBI36
NG_011723.1:g.487784C>T
NG_011723.2:g.487784C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1620C>T (ZFPM2) MANE Select	ENSP00000384179.2:p.Tyr540=
ENST00000407775.6:c.1620C>T (ZFPM2)	ENSP00000384179.2:p.Tyr540=
ENST00000517361.1:c.1224C>T (ZFPM2)	ENSP00000428720.1:p.Tyr408=
ENST00000520492.5:c.1224C>T (ZFPM2)	ENSP00000430757.1:p.Tyr408=
ENST00000522296.1:n.1414C>T (ZFPM2)
NM_012082.3:c.1620C>T (ZFPM2)	NP_036214.2:p.Tyr540=
NR_125796.1:n.180-3260G>A (ZFPM2-AS1)
NR_125797.1:n.191-3260G>A (ZFPM2-AS1)
XM_011516946.1:c.1659C>T (ZFPM2)	XP_011515248.1:p.Tyr553=
XM_011516947.1:c.1590C>T (ZFPM2)	XP_011515249.1:p.Tyr530=
XM_011516948.1:c.1461C>T (ZFPM2)	XP_011515250.1:p.Tyr487=
XM_011516949.1:c.1452C>T (ZFPM2)	XP_011515251.1:p.Tyr484=
NM_001362836.1:c.1461C>T (ZFPM2)	NP_001349765.1:p.Tyr487=
NM_001362837.1:c.1224C>T (ZFPM2)	NP_001349766.1:p.Tyr408=
XM_011516947.3:c.1590C>T (ZFPM2)	XP_011515249.1:p.Tyr530=
NM_012082.4:c.1620C>T (ZFPM2) MANE Select	NP_036214.2:p.Tyr540=
NM_001362836.2:c.1461C>T (ZFPM2)	NP_001349765.1:p.Tyr487=
NM_001362837.2:c.1224C>T (ZFPM2)	NP_001349766.1:p.Tyr408=