Canonical Allele Identifier: CA845059162

Gene: ZFPM2

Linked Data

• dbSNP Id: rs1273901654
• MyVariant Identifiers: chr8:g.106449702T>C (hg19) ; chr8:g.105437474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105437474T>C , CM000670.2:g.105437474T>C	GRCh38
NC_000008.10:g.106449702T>C , CM000670.1:g.106449702T>C	GRCh37
NC_000008.9:g.106518878T>C	NCBI36
NG_011723.1:g.123556T>C
NG_011723.2:g.123556T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.200-6806T>C MANE Select	ENSP00000384179.2:n.200-6806T>C
ENST00000407775.6:c.200-6806T>C	ENSP00000384179.2:n.200-6806T>C
ENST00000511341.6:n.940-6806T>C
ENST00000520027.5:c.-197-6806T>C	ENSP00000428149.1:n.-197-6806T>C
ENST00000520492.5:c.-197-6806T>C	ENSP00000430757.1:n.-197-6806T>C
ENST00000522160.1:n.160-6806T>C
ENST00000524235.5:n.413-6806T>C
NM_012082.3:c.200-6806T>C	NP_036214.2:n.200-6806T>C
XM_011516946.1:c.239-6806T>C	XP_011515248.1:n.239-6806T>C
XM_011516947.1:c.170-6806T>C	XP_011515249.1:n.170-6806T>C
XM_011516948.1:c.41-6806T>C	XP_011515250.1:n.41-6806T>C
XM_011516949.1:c.239-6806T>C	XP_011515251.1:n.239-6806T>C
NM_001362836.1:c.41-6806T>C	NP_001349765.1:n.41-6806T>C
NM_001362837.1:c.-197-6806T>C	NP_001349766.1:n.-197-6806T>C
XM_011516947.3:c.170-6806T>C	XP_011515249.1:n.170-6806T>C
NM_012082.4:c.200-6806T>C MANE Select	NP_036214.2:n.200-6806T>C
NM_001362836.2:c.41-6806T>C	NP_001349765.1:n.41-6806T>C
NM_001362837.2:c.-197-6806T>C	NP_001349766.1:n.-197-6806T>C