Canonical Allele Identifier: CA183188311

Gene: ZFPM2

Linked Data

• dbSNP Id: rs761329032
• gnomAD v3: 8-105497709-G-A
• gnomAD v4: 8-105497709-G-A
• MyVariant Identifiers: chr8:g.106509937G>A (hg19) ; chr8:g.105497709G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105497709G>A , CM000670.2:g.105497709G>A	GRCh38
NC_000008.10:g.106509937G>A , CM000670.1:g.106509937G>A	GRCh37
NC_000008.9:g.106579113G>A	NCBI36
NG_011723.1:g.183791G>A
NG_011723.2:g.183791G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.301+53328G>A MANE Select	ENSP00000384179.2:n.301+53328G>A
ENST00000407775.6:c.301+53328G>A	ENSP00000384179.2:n.301+53328G>A
ENST00000511341.6:n.1041+53328G>A
ENST00000520027.5:c.-96+53328G>A	ENSP00000428149.1:n.-96+53328G>A
ENST00000520492.5:c.-96+53328G>A	ENSP00000430757.1:n.-96+53328G>A
ENST00000524235.5:n.514+53328G>A
NM_012082.3:c.301+53328G>A	NP_036214.2:n.301+53328G>A
XM_011516946.1:c.340+53328G>A	XP_011515248.1:n.340+53328G>A
XM_011516947.1:c.271+53328G>A	XP_011515249.1:n.271+53328G>A
XM_011516948.1:c.142+53328G>A	XP_011515250.1:n.142+53328G>A
XM_011516949.1:c.340+53328G>A	XP_011515251.1:n.340+53328G>A
NM_001362836.1:c.142+53328G>A	NP_001349765.1:n.142+53328G>A
NM_001362837.1:c.-96+53328G>A	NP_001349766.1:n.-96+53328G>A
XM_011516947.3:c.271+53328G>A	XP_011515249.1:n.271+53328G>A
NM_012082.4:c.301+53328G>A MANE Select	NP_036214.2:n.301+53328G>A
NM_001362836.2:c.142+53328G>A	NP_001349765.1:n.142+53328G>A
NM_001362837.2:c.-96+53328G>A	NP_001349766.1:n.-96+53328G>A