Canonical Allele Identifier: CA930277364

Gene: ZMIZ1

Linked Data

• dbSNP Id: rs1032998811
• gnomAD v3: 10-79200232-C-T
• gnomAD v4: 10-79200232-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79200232C>T , CM000672.2:g.79200232C>T	GRCh38
NC_000010.10:g.80959989C>T , CM000672.1:g.80959989C>T	GRCh37
NC_000010.9:g.80629995C>T	NCBI36
NG_028289.1:g.136198C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334512.10:c.-49-1352C>T MANE Select	ENSP00000334474.5:n.-49-1352C>T
ENST00000334512.9:c.-49-1352C>T	ENSP00000334474.5:n.-49-1352C>T
NM_020338.3:c.-49-1352C>T	NP_065071.1:n.-49-1352C>T
XM_005269987.3:c.-49-1352C>T	XP_005270044.1:n.-49-1352C>T
XM_005269988.2:c.-49-1352C>T	XP_005270045.1:n.-49-1352C>T
XM_006717923.2:c.-49-1352C>T	XP_006717986.1:n.-49-1352C>T
XM_006717924.2:c.-49-1352C>T	XP_006717987.1:n.-49-1352C>T
XM_006717925.2:c.-49-1352C>T	XP_006717988.1:n.-49-1352C>T
XM_005269987.5:c.-49-1352C>T	XP_005270044.1:n.-49-1352C>T
XM_005269988.3:c.-49-1352C>T	XP_005270045.1:n.-49-1352C>T
XM_006717923.3:c.-49-1352C>T	XP_006717986.1:n.-49-1352C>T
XM_006717924.3:c.-49-1352C>T	XP_006717987.1:n.-49-1352C>T
XM_006717925.3:c.-49-1352C>T	XP_006717988.1:n.-49-1352C>T
NM_020338.4:c.-49-1352C>T MANE Select	NP_065071.1:n.-49-1352C>T