Canonical Allele Identifier: CA4839632

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 700577
• ClinVar RCV Id: RCV000868816
• dbSNP Id: rs370717147
• ExAC: 8:106810948 G / T
• gnomAD v4: 8-105798720-G-T
• MyVariant Identifiers: chr8:g.106810948G>T (hg19) ; chr8:g.105798720G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105798720G>T , CM000670.2:g.105798720G>T	GRCh38
NC_000008.10:g.106810948G>T , CM000670.1:g.106810948G>T	GRCh37
NC_000008.9:g.106880124G>T	NCBI36
NG_011723.1:g.484802G>T
NG_011723.2:g.484802G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.740-4G>T (ZFPM2) MANE Select	ENSP00000384179.2:n.740-4G>T
ENST00000407775.6:c.740-4G>T (ZFPM2)	ENSP00000384179.2:n.740-4G>T
ENST00000517361.1:c.344-4G>T (ZFPM2)	ENSP00000428720.1:n.344-4G>T
ENST00000520492.5:c.344-4G>T (ZFPM2)	ENSP00000430757.1:n.344-4G>T
ENST00000522296.1:n.534-4G>T (ZFPM2)
NM_012082.3:c.740-4G>T (ZFPM2)	NP_036214.2:n.740-4G>T
NR_125796.1:n.180-278C>A (ZFPM2-AS1)
NR_125797.1:n.191-278C>A (ZFPM2-AS1)
XM_011516946.1:c.779-4G>T (ZFPM2)	XP_011515248.1:n.779-4G>T
XM_011516947.1:c.710-4G>T (ZFPM2)	XP_011515249.1:n.710-4G>T
XM_011516948.1:c.581-4G>T (ZFPM2)	XP_011515250.1:n.581-4G>T
XM_011516949.1:c.572-4G>T (ZFPM2)	XP_011515251.1:n.572-4G>T
NM_001362836.1:c.581-4G>T (ZFPM2)	NP_001349765.1:n.581-4G>T
NM_001362837.1:c.344-4G>T (ZFPM2)	NP_001349766.1:n.344-4G>T
XM_011516947.3:c.710-4G>T (ZFPM2)	XP_011515249.1:n.710-4G>T
NM_012082.4:c.740-4G>T (ZFPM2) MANE Select	NP_036214.2:n.740-4G>T
NM_001362836.2:c.581-4G>T (ZFPM2)	NP_001349765.1:n.581-4G>T
NM_001362837.2:c.344-4G>T (ZFPM2)	NP_001349766.1:n.344-4G>T